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rs13088462

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs13088462(C;C)
Make rs13088462(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position51034282
GeneDOCK3
is asnp
is mentioned by
dbSNPrs13088462
ebirs13088462
HLIrs13088462
Exacrs13088462
Varsomers13088462
Maprs13088462
PheGenIrs13088462
hapmaprs13088462
1000 genomesrs13088462
hgdprs13088462
ensemblrs13088462
gopubmedrs13088462
geneviewrs13088462
scholarrs13088462
googlers13088462
pharmgkbrs13088462
gwascentralrs13088462
openSNPrs13088462
23andMers13088462
23andMe allrs13088462
SNP Nexus

SNPshotrs13088462
SNPdbers13088462
MSV3drs13088462
GWAS Ctlgrs13088462
GMAF0.01837
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 4E-10
Odds Ratio 0.0500 [NR] meters decrease