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rs117096873

From SNPedia

Orientationplus
Stabilizedplus
Make rs117096873(C;C)
Make rs117096873(C;T)
Make rs117096873(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position11293103
is asnp
is mentioned by
dbSNPrs117096873
ebirs117096873
HLIrs117096873
Exacrs117096873
Varsomers117096873
Maprs117096873
PheGenIrs117096873
hapmaprs117096873
1000 genomesrs117096873
hgdprs117096873
ensemblrs117096873
gopubmedrs117096873
geneviewrs117096873
scholarrs117096873
googlers117096873
pharmgkbrs117096873
gwascentralrs117096873
openSNPrs117096873
23andMers117096873
23andMe allrs117096873
SNP Nexus

SNPshotrs117096873
SNPdbers117096873
MSV3drs117096873
GWAS Ctlgrs117096873
GMAF0.006428
Max Magnitude
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Bulimia nervosa
Title Genetic variants associated with disordered eating.
Risk Allele C
P-val 2E-6
Odds Ratio .13 [0.076-0.182] unit decrease