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rs16910061

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs16910061(A;A)
Make rs16910061(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position94552459
is asnp
is mentioned by
dbSNPrs16910061
dbSNP (classic)rs16910061
ClinGenrs16910061
ebirs16910061
HLIrs16910061
Exacrs16910061
Gnomadrs16910061
Varsomers16910061
LitVarrs16910061
Maprs16910061
PheGenIrs16910061
Biobankrs16910061
1000 genomesrs16910061
hgdprs16910061
ensemblrs16910061
geneviewrs16910061
scholarrs16910061
googlers16910061
pharmgkbrs16910061
gwascentralrs16910061
openSNPrs16910061
23andMers16910061
SNPshotrs16910061
SNPdbers16910061
MSV3drs16910061
GWAS Ctlgrs16910061
GMAF0.0753
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 19893584]
Trait Height
Title Identification of 15 loci influencing height in a Korean population
Risk Allele T
P-val 0.000003
Odds Ratio 0.53 [NR] cm decrease