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rs9313296

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs9313296(C;C)
Make rs9313296(C;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position165950694
is asnp
is mentioned by
dbSNPrs9313296
dbSNP (classic)rs9313296
ClinGenrs9313296
ebirs9313296
HLIrs9313296
Exacrs9313296
Gnomadrs9313296
Varsomers9313296
LitVarrs9313296
Maprs9313296
PheGenIrs9313296
Biobankrs9313296
1000 genomesrs9313296
hgdprs9313296
ensemblrs9313296
geneviewrs9313296
scholarrs9313296
googlers9313296
pharmgkbrs9313296
gwascentralrs9313296
openSNPrs9313296
23andMers9313296
SNPshotrs9313296
SNPdbers9313296
MSV3drs9313296
GWAS Ctlgrs9313296
GMAF0.1042
Max Magnitude0
? (C;C) (C;G) (G;G) 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 C
P-val 7E-7
Odds Ratio 10.0000 [6.07-13.93] kg increase