Have questions? Visit https://www.reddit.com/r/SNPedia

rs9906155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs9906155(C;C)
Make rs9906155(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position77705615
is asnp
is mentioned by
dbSNPrs9906155
ebirs9906155
HLIrs9906155
Exacrs9906155
Varsomers9906155
Maprs9906155
PheGenIrs9906155
hapmaprs9906155
1000 genomesrs9906155
hgdprs9906155
ensemblrs9906155
gopubmedrs9906155
geneviewrs9906155
scholarrs9906155
googlers9906155
pharmgkbrs9906155
gwascentralrs9906155
openSNPrs9906155
23andMers9906155
23andMe allrs9906155
SNP Nexus

SNPshotrs9906155
SNPdbers9906155
MSV3drs9906155
GWAS Ctlgrs9906155
GMAF0.0427
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20966902OA-icon.png]
Trait
Title Genome-Wide Association Study of Anthropometric Traits and Evidence of Interactions With Age and Study Year in Filipino Women
Risk Allele T
P-val 0.000009
Odds Ratio 0.0500 [0.02-0.07] unit increase