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rs8002779

From SNPedia

Orientationplus
Stabilizedplus
Make rs8002779(A;A)
Make rs8002779(A;G)
Make rs8002779(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position91363723
GeneLOC107984617
is asnp
is mentioned by
dbSNPrs8002779
dbSNP (classic)rs8002779
ClinGenrs8002779
ebirs8002779
HLIrs8002779
Exacrs8002779
Gnomadrs8002779
Varsomers8002779
LitVarrs8002779
Maprs8002779
PheGenIrs8002779
Biobankrs8002779
1000 genomesrs8002779
hgdprs8002779
ensemblrs8002779
geneviewrs8002779
scholarrs8002779
googlers8002779
pharmgkbrs8002779
gwascentralrs8002779
openSNPrs8002779
23andMers8002779
SNPshotrs8002779
SNPdbers8002779
MSV3drs8002779
GWAS Ctlgrs8002779
GMAF0.4908
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 A
P-val 0.000003
Odds Ratio 0.05 [0.03-0.07] cm decrease