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rs6473015

From SNPedia

Orientationplus
Stabilizedplus
Make rs6473015(A;A)
Make rs6473015(A;C)
Make rs6473015(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position77266249
is asnp
is mentioned by
dbSNPrs6473015
dbSNP (classic)rs6473015
ClinGenrs6473015
ebirs6473015
HLIrs6473015
Exacrs6473015
Gnomadrs6473015
Varsomers6473015
LitVarrs6473015
Maprs6473015
PheGenIrs6473015
Biobankrs6473015
1000 genomesrs6473015
hgdprs6473015
ensemblrs6473015
geneviewrs6473015
scholarrs6473015
googlers6473015
pharmgkbrs6473015
gwascentralrs6473015
openSNPrs6473015
23andMers6473015
SNPshotrs6473015
SNPdbers6473015
MSV3drs6473015
GWAS Ctlgrs6473015
GMAF0.2204
Max Magnitude0
? (A;A) (A;C) (C;C) 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 7E-13
Odds Ratio .03 [NR] unit decrease