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rs11170631

From SNPedia

Orientationplus
Stabilizedplus
Make rs11170631(C;C)
Make rs11170631(C;T)
Make rs11170631(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position53647408
is asnp
is mentioned by
dbSNPrs11170631
ebirs11170631
HLIrs11170631
Exacrs11170631
Varsomers11170631
Maprs11170631
PheGenIrs11170631
hapmaprs11170631
1000 genomesrs11170631
hgdprs11170631
ensemblrs11170631
gopubmedrs11170631
geneviewrs11170631
scholarrs11170631
googlers11170631
pharmgkbrs11170631
gwascentralrs11170631
openSNPrs11170631
23andMers11170631
23andMe allrs11170631
SNP Nexus

SNPshotrs11170631
SNPdbers11170631
MSV3drs11170631
GWAS Ctlgrs11170631
GMAF0.4275
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20189936]
Trait Height
Title A genome-wide association study in 19,633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci
Risk Allele C
P-val 9E-7
Odds Ratio 0.05 [0.03-0.07] cm increase