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rs7971536

From SNPedia

Orientationplus
Stabilizedplus
Make rs7971536(A;A)
Make rs7971536(A;T)
Make rs7971536(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position101980010
is asnp
is mentioned by
dbSNPrs7971536
ebirs7971536
HLIrs7971536
Exacrs7971536
Varsomers7971536
Maprs7971536
PheGenIrs7971536
hapmaprs7971536
1000 genomesrs7971536
hgdprs7971536
ensemblrs7971536
gopubmedrs7971536
geneviewrs7971536
scholarrs7971536
googlers7971536
pharmgkbrs7971536
gwascentralrs7971536
openSNPrs7971536
23andMers7971536
23andMe allrs7971536
SNP Nexus

SNPshotrs7971536
SNPdbers7971536
MSV3drs7971536
GWAS Ctlgrs7971536
GMAF0.4004
Max Magnitude
? (A;A) (A;T) (T;T) 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 A
P-val 8E-14
Odds Ratio 0.03 [NR] unit decrease