SNPs

Related by string. SNP * * SNP councilor . Lib Dem SNP . SNP Lib Dem . SNP rs# [001] . SNP MSP . SNP manifesto . SNP MSPs . SNP MSP Christine . Sinopec SNP . Alex Salmond SNP . Synopsys SNPS . SNP Holyrood . Synopsys NASDAQ SNPS . SNP Alex Salmond . genome SNPs conferring . Inc. Nasdaq SNPS . SNP genotyping . Inc. NASDAQ SNPS . SNPs pronounced snips . Inc SNPS . SNP Array #.# . SNP Genotyping *

Related by context. All words. (Click for frequent words.) 74 genetic variants 74 polymorphisms 74 single nucleotide polymorphisms 72 single nucleotide polymorphism 71 genetic variations 71 loci 71 haplotypes 71 CNVs 70 gene variants 69 genetic markers 68 haplotype 68 rs# [003] 66 genomes 66 alleles 66 genotypes 65 mutations 65 rs# [002] 65 genes 65 #q# [001] 65 genome 65 genotype 65 susceptibility genes 64 genotyped 64 polymorphism 63 #q# [002] 63 gene mutations 63 microdeletions 63 genetic variation 63 chromosome #q# [001] 63 phenotypes 63 chromosome #q# [002] 62 linkage disequilibrium 62 indels 62 DNA sequences 62 genomic 62 rs# [001] 62 miRNAs 62 gene expression 62 chromosome #p# [001] 61 genetic polymorphisms 61 transcriptome 61 #p# [001] 60 chromosomal regions 60 genetic loci 60 missense mutations 60 susceptibility gene 60 genetic mutations 60 genetic variants associated 60 allele frequencies 60 nucleotide sequence 60 SNPs pronounced snips 60 mutation 60 gene 60 biomarkers 60 EGFR mutations 60 sporadic ALS 59 exons 59 genomewide 59 exomes 59 human genome 59 genetic variant 59 PALB2 59 microRNA expression 59 chromosomal 59 gene expression profiles 59 susceptibility loci 59 gene variant 59 somatic mutations 59 apolipoprotein E gene 58 phenotype 58 heterozygous 58 rs# [004] 58 biomarker 58 microRNAs 58 coding sequences 58 #S rRNA 58 allelic 58 MLH1 58 mutated genes 58 microarray experiments 58 array CGH 58 autosomal 58 APOE e4 58 homozygosity 57 UTRs 57 homozygous 57 miRNA expression 57 MYH9 57 TCF#L# 57 MYH9 gene 57 gene mutation 57 TCF#L# gene 57 nucleotide 57 GSTP1 57 chromosome #p#.# 57 splice junctions 57 causal variants 57 PTPN# 57 intergenic 57 germline mutations 57 chromosome 57 micro RNA 57 #p#.# [001] 57 ALK mutations 57 chromosomal abnormalities 57 SNP rs# [001] 57 mtDNA 56 intron 56 genotyping 56 protein coding 56 gene expression patterns 56 #q#.# [002] 56 chromosomal rearrangements 56 phenotypic variation 56 VKORC1 56 PICALM 56 inherited mutations 56 kilobase 56 chromosome #q#.# [001] 56 mitochondrial gene 56 gene polymorphisms 56 #q#.# [001] 56 FMR1 gene 56 orthologs 56 genetic 56 clusterin 56 heterozygotes 56 pathogenic mutations 56 variant allele 56 PTEN mutations 56 MTHFR 56 KIAA# 56 MSH2 56 allele 56 autism susceptibility genes 56 yeast genome 56 segmental duplications 56 intronic 56 LRRK2 gene 56 PCa 56 quantitative trait loci 56 mitochondrial genome 55 #p# [003] 55 genotyping arrays 55 C#Y 55 miRNA 55 molecular markers 55 5 HTTLPR 55 genetic abnormalities 55 codons 55 chromosome #q 55 methylation 55 gene locus 55 FGFR2 55 exon 55 coding exons 55 heterozygosity 55 genotypic 55 Venter genome 55 genes CYP#C# 55 colorectal neoplasia 55 BRCA1 55 CHEK2 55 methylation patterns 55 genomewide association studies 55 miRNA genes 55 CDH1 55 bacterial genomes 55 kilobases 55 BARD1 55 splice variants 55 gene fusions 55 GSTM1 55 mRNA expression 55 transcriptomes 55 microarray 55 DNA methylation 55 CDKN2A 55 imprinted genes 54 APOL1 54 APOE 54 microsatellite markers 54 genetic alterations 54 IL#B 54 HapMap 54 indel 54 aCGH 54 APOE gene 54 nucleotide substitutions 54 gene variation 54 genomic DNA 54 karyotype 54 chromosome #p# [002] 54 paralogs 54 subtypes 54 MC1R gene 54 T2D 54 BRCA2 mutation 54 SNP Array #.# 54 cytogenetic 54 mRNA transcripts 54 homologs 54 VNTR 54 transcriptome sequencing 54 spontaneous mutations 54 gene loci 54 proteome 54 insertions deletions 54 genes encoding 54 causative mutations 54 kinases 54 NAFLD 54 Alu elements 54 conserved sequences 54 aneuploidies 54 BRCA1 mutations 54 HLA DRB1 54 familial ALS 54 DRD2 54 KRAS mutations 54 LQTS 54 Arabidopsis genes 54 sequenced genomes 54 CNTNAP2 54 Haplotype 54 BRCA mutations 54 RNA sequences 54 adenoma 54 NNRTI resistance 54 KRAS mutation 54 amplicons 54 hypermethylated 54 promoter methylation 54 ZNF# 53 genomic loci 53 noncoding RNAs 53 International HapMap Project 53 heritable 53 alternatively spliced 53 familial pancreatic cancer 53 breast cancer genes BRCA1 53 differentially expressed genes 53 susceptibility locus 53 mRNAs 53 protein isoforms 53 mtDNA mutations 53 phenotypic 53 activating mutation 53 HNPCC 53 mutated gene 53 haplogroups 53 RASSF1A 53 genomic variants 53 ultraconserved elements 53 tumor suppressor gene 53 subtype 53 CC genotype 53 genetic determinants 53 mammalian genome 53 T2DM 53 microRNA 53 APOE4 53 proband 53 microcephalin 53 ERBB2 53 TGFBR1 * 6A 53 dbSNP 53 ABCB1 53 exome 53 SORL1 gene 53 CYP#D# gene 53 HLA genes 53 genetic makeup 53 Single Nucleotide Polymorphism 53 recombination hotspots 53 IL#R 53 SORL1 53 NPY gene 53 #p#.# [002] 53 virulence genes 53 RNA transcripts 53 TOMM# 53 X chromosome 53 lung adenocarcinoma 53 TACI mutations 53 LPA gene 53 splice variant 53 genomic variation 53 mammalian genomes 53 DRD2 gene 53 probands 53 uncharacterized genes 53 MGUS 53 microarray analysis 53 SLC#A# [001] 53 penetrance 53 variant rs# 53 K ras mutations 53 pseudogenes 53 shRNAs 53 mitochondrial DNA mtDNA 53 hypermethylation 53 HMGA2 53 coding genes 53 differentially expressed proteins 53 whole genome genotyping 53 QTLs 53 gene amplification 53 nucleotide sequences 53 SNP arrays 53 chromosomal rearrangement 53 CGG repeats 53 PTEN gene 53 cDNAs 53 MC1R 52 microdeletion 52 perilipin 52 TT genotype 52 Sanger sequencing 52 autoantibodies 52 alternative splicing 52 aberrant methylation 52 mammographic density 52 genetic locus 52 MAPK pathway 52 MDM2 52 Chromosome 52 cystatin C 52 CpG 52 phylogenetic analyzes 52 HLA B# 52 gene encoding 52 sequence homology 52 EGFR gene 52 BRCA1 gene 52 Genotypes 52 FLT3 52 micro RNAs 52 missense mutation 52 monogenic 52 SNP genotyping 52 endometrial cancers 52 non coding RNAs 52 isoforms 52 microsatellite instability 52 KIF6 gene 52 Single Nucleotide Polymorphisms 52 FMR1 52 PRNP 52 ApoE gene 52 intergenic regions 52 WT1 52 ApoE 52 PIK3CA 52 WTCCC 52 BRCA2 52 proteins 52 MTHFR gene 52 metabolic syndrome 52 homologues 52 Single Nucleotide Polymorphisms SNPs 52 chromosomes 52 HOTAIR 52 oligonucleotide probes 52 HumanHap# BeadChip 52 breast cancer susceptibility genes 52 FTLD 52 gene APOE 52 narcolepsy cataplexy 52 SLC#A# [002] 52 molecular abnormalities 52 sarcosine 52 variants 52 COL#A# 52 ChIP chip 52 BRAF mutations 52 de novo mutations 52 TMEM#B 52 breast carcinomas 52 VHL gene 52 human genome SNPs 52 microRNA molecules 52 breast cancer subtypes 52 rs# rs# 52 enterotypes 52 genes predisposing 52 FTO gene 52 HAAH 52 noncoding 52 allelic variants 52 Arabidopsis genome 52 Genotype 52 CYP# [002] 52 amino acid substitutions 52 allelic variation 51 histone modifications 51 methylated DNA 51 cognitively normal 51 dysbindin 51 PALB2 gene 51 causative gene 51 amino acid sequences 51 CYP#C# [001] 51 Lp PLA2 51 Clusterin 51 chromosome #q#.# [002] 51 exfoliation glaucoma 51 NF1 gene 51 OGG1 51 genomic sequences 51 primate genomes 51 contigs 51 BRAF V#E 51 adenocarcinomas 51 unmethylated 51 MIF protein 51 MetS 51 studies GWAS 51 lymphoblastoid cell lines 51 maize genome 51 mutational analysis 51 KRAS oncogene 51 IgA deficiency 51 SLC#A# gene [001] 51 proteomes 51 cDNA libraries 51 MLL2 51 qRT PCR 51 G allele 51 rRNA 51 microarrays 51 BRCA1 BRCA2 51 RNAs 51 prediabetes 51 biological pathways 51 IGFBP 51 advanced adenomas 51 chromosomal aberrations 51 monozygotic twins 51 genetic ancestry 51 DNA methylation patterns 51 molecular subtypes 51 histone modification 51 DQB1 * 51 ependymomas 51 NSCLC tumors 51 cardioembolic stroke 51 telomere lengths 51 Genetic variants 51 chimpanzee genomes 51 genetic mutation 51 APOE ε4 51 lymph node metastases 51 Genomes Project 51 causative mutation 51 benign lesions 51 SNP rs# [002] 51 genes BRCA1 51 amino acid sequence 51 ORMDL3 51 gene expression assays 51 genetic sequences 51 susceptibility alleles 51 differential gene expression 51 elevated CRP 51 apolipoprotein E 51 CYP#C# [002] 51 human leukocyte antigen 51 nondiabetic 51 alpha synuclein gene 51 non coding RNA 51 microbial genomes 51 genome sequences 51 protein kinases 51 amino acid substitution 51 OCA2 51 untranslated regions 51 ChIP Seq 51 TMPRSS2 ERG 51 dopamine receptor gene 51 pyrosequencing 51 BRCA mutation 51 dopamine transporter gene 51 epigenetic 51 molecular biomarkers 51 KLF4 51 KRAS 51 familial clustering 51 medulloblastomas 51 Recurrence Score 51 subclinical hyperthyroidism 51 endophenotypes 50 genome rearrangements 50 OPRM1 gene 50 homozygotes 50 logistic regression analysis 50 MicroRNA 50 SMAD4 50 UGT#B# 50 HMGA2 gene 50 IKZF1 50 sCJD 50 #q# deletion 50 chromosomal instability 50 variant alleles 50 NF1 50 amino acid residues 50 CpG islands 50 MHC molecules 50 basal cell nevus syndrome 50 overexpression 50 malignant nodules 50 prostate cancer CaP 50 amplicon 50 genetic aberrations 50 HNSCC 50 evolutionarily conserved 50 chromatin immunoprecipitation ChIP 50 vimentin 50 HPV# 50 TRAF1 C5 50 genomic alterations 50 kinase 50 telomere length 50 CFH gene 50 tumor suppressor genes 50 LRRK2 mutation 50 R#W [002] 50 ORFs 50 underlying pathophysiology 50 albuminuria 50 receptor gene 50 BRCA2 gene 50 miR #b [002] 50 nucleotides 50 mutant gene 50 BRCA2 mutations 50 G#S mutation 50 gene expression profiling 50 organism genome 50 colorectal cancer CRC 50 genomic sequence 50 Resequencing 50 chromosomal deletions 50 uPAR 50 comparative genomic hybridization CGH 50 BRCA genes 50 nucleotide variations 50 LRP5 50 epigenomes 50 chromosomal anomalies 50 substrate specificity 50 highly heritable 50 CALHM1 50 #S rDNA 50 APOC3 50 IDH1 mutation 50 chromosomal alterations 50 prion protein gene 50 prognostic marker 50 LRAT 50 GSTT1 50 homology 50 missense 50 HLA DRB1 SE 50 gene rearrangements 50 PITX2 50 cDNA 50 multigenic 50 ortholog 50 A. thaliana 50 RNA Seq 50 APOE e4 gene 50 palladin 50 PFGE 50 peptide sequences 50 insertion deletion 50 hepatocellular carcinomas 50 allele frequency 50 hydroxyvitamin D levels 50 UGT#A# * 50 TOP2A 50 CYP#D# 50 BAC clones 50 ApoE4 gene 50 Wwox 50 TP# gene 50 RNA molecules 50 Drosophila genome 50 autoantibody 50 transfected 50 homozygote 50 comorbidity 50 distinct subtypes 50 modifier genes 50 5 hydroxymethylcytosine 50 frontotemporal dementia 50 APOE genotype 50 prognostic markers 50 TERT 50 comparative genomic hybridization 50 PCR amplified 50 homologous genes 50 generalized vitiligo 50 p# mutations 50 functional polymorphism 50 cytochrome b 50 ncRNAs 50 Microarrays 50 heterozygote 50 epitopes 50 STAT4 50 K ras 50 haplogroup 50 major histocompatibility complex 50 MicroRNAs 50 APOE allele 50 genetic heterogeneity 50 SPINK1 50 subcellular localization 50 BRAF mutation 50 NF2 50 Methylation 50 prognostic factor 50 serotonin receptor 50 TMPRSS2 ERG fusion 50 heritable traits 50 MSH6 50 platypus genome 50 mutant alleles 50 serous ovarian cancer 50 atypical hyperplasia 50 CAG repeats 50 Jhdm2a 50 ADPKD 50 activating mutations 50 HFE gene 50 CYP#E# gene 50 microRNAs miRNAs 50 CagA 49 ADRB2 49 inbred strains 49 aneuploidy 49 lincRNAs 49 hierarchical clustering 49 kinase inhibitors 49 genes differentially expressed 49 YKL 49 TSC1 49 transcriptomic 49 histopathologic 49 M. genitalium 49 Genetic variations 49 subclinical atherosclerosis 49 extracolonic findings 49 transcriptional profiles 49 elevated triglyceride levels 49 mRNA molecules 49 number variation CNV 49 glycoproteins 49 tumor suppressor protein 49 adenomas 49 Cytogenetic 49 3'UTR 49 3' UTR 49 Haptoglobin 49 SCN5A 49 HLA molecules 49 synuclein 49 FGFR3 49 mutational 49 genomic deletions 49 cDNA microarray 49 PARP inhibition 49 GBM tumors 49 methylenetetrahydrofolate reductase 49 DRD4 49 vitamin D receptor 49 bisulfite sequencing 49 ApoE4 49 LRRK2 49 WNK1 49 endostatin 49 PDE#A 49 #S rRNA gene 49 CFTR gene 49 gene sequences 49 FGFR1 49 endogenous retroviruses 49 phenotypically 49 apoE 49 Li Fraumeni syndrome 49 MHC genes 49 autosomal dominant 49 microalbuminuria 49 operon 49 causative genes 49 epithelial tumors 49 KRAS gene 49 transcription factors 49 Polymorphisms 49 codon 49 nestin 49 TCF4 49 fasting glucose 49 mutated K ras 49 Heterozygous 49 maternally inherited 49 CDK4 49 MECP2 gene 49 5q 49 BCR ABL 49 ALK gene 49 zebrafish genome 49 HLA DRB1 * 49 ribosomal protein 49 transposable elements 49 genetic susceptibility 49 familial aggregation 49 lymph node metastasis 49 circadian genes 49 thyrotropin levels 49 phenotypic traits 49 transcriptional 49 Microarray 49 MC4R 49 FASPS 49 EGFR mutation 49 HER2 gene 49 TIMP 1 49 HLA DQ2 49 number variations CNVs 49 cardiac troponin T 49 phenotypic differences 49 advanced neoplasia 49 H#K#me# 49 metabolomic 49 HDACs 49 Whole Genome 49 chromosomal translocations 49 repeat allele 49 resequencing 49 adiponectin concentrations 49 microRNA biomarkers 49 evolutionary conserved 49 protein encoded 49 ADAM# 49 TP# mutation 49 protein biomarkers 49 NR#A# gene 49 neurofibromatosis type 49 TP# mutations 49 fungal genomes 49 promoter hypermethylation 49 tumor biopsies 49 SMN2 gene 49 heritability 49 UCRs 49 gene APOE4 49 mammalian organisms 49 genomic rearrangements 49 IDH1 49 MSMB 49 poor metabolizers 49 Multiple logistic regression 49 miRs 49 epigenetic mechanisms 49 somatic mutation 49 NGAL 49 frameshift mutation 49 mutant allele 49 BeadChip 49 ALDH2 49 hereditary hemochromatosis 49 DeCode 49 CPE delta N 49 tumor suppressor 49 megabases 49 HLA alleles 49 segmental duplication 49 MC4R gene 48 ChIP seq 48 multivariate analyzes 48 Sjögren syndrome 48 ubiquitinated 48 Ashkenazi Jewish 48 HLA B 48 BDNF gene 48 paternally inherited 48 introns 48 colorectal cancers 48 microarray gene expression 48 DLC1 48 nonsense mutations 48 subclinical 48 odorant receptor 48 diploid genome 48 phylogenetically 48 HER3 48 transmembrane proteins 48 transcriptional regulation 48 5 hmC 48 CGH arrays 48 survivin 48 chromosomal anomaly 48 LIS1 48 primary biliary cirrhosis 48 AAT deficiency 48 isotype 48 genetic variability 48 dizygotic twins 48 clade B 48 immunohistochemical 48 conditional logistic regression 48 viral genome 48 RNA seq 48 breast cancer metastasis 48 immunofluorescent 48 S#A# [002] 48 mRNA 48 body louse genome 48 white matter hyperintensities 48 operons 48 NFKBIA 48 orthologous 48 GPC5 48 IGF2 48 CYP#E# 48 gigabases 48 CHI#L# 48 tyrosine phosphorylation 48 colorectal polyps 48 EoE 48 receptor kinase 48 HLA DQ 48 cyclin E 48 VIPR2 48 immunoglobulin genes 48 transcriptional profiling 48 molecular pathways 48 HPV genotypes 48 CISH 48 epitope 48 colorectal carcinoma 48 DLX5 48 GLI1 48 c Myb 48 HLA DR 48 chimp genome 48 genetic traits 48 pilocytic astrocytomas 48 multigene 48 advanced adenoma 48 miR #a [001] 48 subfamilies 48 polygenic 48 mosaicism 48 gene polymorphism 48 mitogen activated protein kinase 48 parkin gene 48 SNCA 48 MLL gene 48 comorbidities 48 CpG island 48 KCNQ1 48 logistic regression model 48 FDG PET 48 tyrosine kinases 48 subpopulations 48 K ras gene 48 B7 H3 48 GSTM1 gene 48 clinicopathological 48 galectin 3 48 immunohistochemical staining 48 multiplex ligation dependent 48 miRNA expression patterns 48 CNTNAP2 gene 48 K#R [002] 48 Hakonarson 48 fraternal twin pairs 48 small RNAs 48 genomic instability 48 INF2 48 P. falciparum 48 protein 48 rDNA 48 EphB4 48 epistasis 48 E#F# 48 BMP2 48 recessive mutations 48 Genetic variation 48 HDAC 48 BRCA1 mutation carriers 48 chromosome aberrations 48 colorectal neoplasms 48 PON1 48 MRSA isolates 48 high throughput sequencing 48 RUNX3 48 BRAF gene 48 thymine 48 Li Fraumeni 48 exome sequencing 48 proto oncogene 48 genetic modifiers 48 Axiom Genomic Database 48 SMN2 48 GBA mutations 48 genetic abnormality 48 familial predisposition 48 transmembrane 48 HumanHap# 48 genetic polymorphism 48 STK# gene 48 polyadenylation 48 guanine G 48 subfamily 48 suppressor gene 48 aggrecan 48 biochemical marker 48 Cyclin E 48 S. maltophilia 48 matrix metalloproteinase 48 apoE4 48 clades 48 APOE e4 allele 48 ribosomal RNA 48 Supplementary Table 48 Apolipoprotein E 48 cis regulatory 48 cytokeratin 48 karyotyping 48 GABRA2 48 JAK2 V#F 48 colon cancers 48 troponin T 48 oncogenic 48 lipid abnormalities 48 amyloidogenic 48 micrometastases 48 Human SNP Array 48 lipoprotein 48 Phenotype 48 APOE4 gene 48 predictive biomarker 48 kaempferol 48 Polymorphism 48 CCL#L# 48 cystatin 48 constitutively 48 Alleles 48 cM 48 oligonucleotide microarray 48 mitochondrial genomes 48 BeadChips 48 morphologic 48 methylated 48 androgen receptor gene 48 BRCA 48 cyclin D1 48 thyroglobulin 48 C#T [002] 48 epigenetic alterations 48 PAK1 48 etiologic 48 HMGCR 47 V#F mutation 47 malignant lesions 47 KIF6 gene variant 47 multiplex PCR 47 isoform 47 SLITRK1 47 differentially expressed 47 number variants CNVs 47 genomewide association study 47 carotid plaque 47 HER2 amplification 47 acetylation 47 gene deletions 47 catechol O methyltransferase 47 haplotype map 47 p# mutation 47 germline mutation 47 QTL mapping 47 epigenetic modification 47 NPM1 mutations 47 biochemical markers 47 miRBase 47 glycan 47 Mutational 47 colorectal tumors 47 stranded nucleic acids 47 CYP#B# 47 gene expression microarrays 47 MAOA gene 47 hepatocellular carcinoma 47 kDa protein

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