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rs11923600

From SNPedia

Orientationplus
Stabilizedplus
Make rs11923600(A;A)
Make rs11923600(A;G)
Make rs11923600(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position176209663
is asnp
is mentioned by
dbSNPrs11923600
dbSNP (classic)rs11923600
ClinGenrs11923600
ebirs11923600
HLIrs11923600
Exacrs11923600
Gnomadrs11923600
Varsomers11923600
LitVarrs11923600
Maprs11923600
PheGenIrs11923600
Biobankrs11923600
1000 genomesrs11923600
hgdprs11923600
ensemblrs11923600
geneviewrs11923600
scholarrs11923600
googlers11923600
pharmgkbrs11923600
gwascentralrs11923600
openSNPrs11923600
23andMers11923600
SNPshotrs11923600
SNPdbers11923600
MSV3drs11923600
GWAS Ctlgrs11923600
GMAF0.2034
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23456168]
Trait Height
Title Genome-wide association study in Han Chinese identifies three novel loci for human height.
Risk Allele G
P-val 8E-6
Odds Ratio .08 [0.047-0.121] unit increase