Have questions? Visit https://www.reddit.com/r/SNPedia

rs961764

From SNPedia

Orientationminus
Stabilizedminus
Make rs961764(C;C)
Make rs961764(C;G)
Make rs961764(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position117200993
is asnp
is mentioned by
dbSNPrs961764
ebirs961764
HLIrs961764
Exacrs961764
Varsomers961764
Maprs961764
PheGenIrs961764
hapmaprs961764
1000 genomesrs961764
hgdprs961764
ensemblrs961764
gopubmedrs961764
geneviewrs961764
scholarrs961764
googlers961764
pharmgkbrs961764
gwascentralrs961764
openSNPrs961764
23andMers961764
23andMe allrs961764
SNP Nexus

SNPshotrs961764
SNPdbers961764
MSV3drs961764
GWAS Ctlgrs961764
GMAF0.3792
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele C
P-val 1E-11
Odds Ratio .02 [NR] unit decrease