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

rs6470764

From SNPedia

Orientationplus
Stabilizedplus
Make rs6470764(C;C)
Make rs6470764(C;T)
Make rs6470764(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position129713419
GeneLOC100130376
is asnp
is mentioned by
dbSNPrs6470764
ebirs6470764
HLIrs6470764
Exacrs6470764
Varsomers6470764
Maprs6470764
PheGenIrs6470764
hapmaprs6470764
1000 genomesrs6470764
hgdprs6470764
ensemblrs6470764
gopubmedrs6470764
geneviewrs6470764
scholarrs6470764
googlers6470764
pharmgkbrs6470764
gwascentralrs6470764
openSNPrs6470764
23andMers6470764
23andMe allrs6470764
SNP Nexus

SNPshotrs6470764
SNPdbers6470764
MSV3drs6470764
GWAS Ctlgrs6470764
GMAF0.4963
Max Magnitude
? (C;C) (C;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 T
P-val 2E-28
Odds Ratio 0.05 [NR] unit decrease