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rs7742369

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs7742369(A;G)
Make rs7742369(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position34197944
is asnp
is mentioned by
dbSNPrs7742369
ebirs7742369
HLIrs7742369
Exacrs7742369
Varsomers7742369
Maprs7742369
PheGenIrs7742369
hapmaprs7742369
1000 genomesrs7742369
hgdprs7742369
ensemblrs7742369
gopubmedrs7742369
geneviewrs7742369
scholarrs7742369
googlers7742369
pharmgkbrs7742369
gwascentralrs7742369
openSNPrs7742369
23andMers7742369
23andMe allrs7742369
SNP Nexus

SNPshotrs7742369
SNPdbers7742369
MSV3drs7742369
GWAS Ctlgrs7742369
GMAF0.2989
Max Magnitude0
? (A;A) (A;G) (G;G) 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 G
P-val 1E-13
Odds Ratio 0.11 [0.08-0.14] cm increase

[PMID 19343178OA-icon.png] Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.