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rs117124364

From SNPedia

Orientationplus
Stabilizedplus
Make rs117124364(C;C)
Make rs117124364(C;T)
Make rs117124364(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position32997453
is asnp
is mentioned by
dbSNPrs117124364
ebirs117124364
HLIrs117124364
Exacrs117124364
Varsomers117124364
Maprs117124364
PheGenIrs117124364
hapmaprs117124364
1000 genomesrs117124364
hgdprs117124364
ensemblrs117124364
gopubmedrs117124364
geneviewrs117124364
scholarrs117124364
googlers117124364
pharmgkbrs117124364
gwascentralrs117124364
openSNPrs117124364
23andMers117124364
23andMe allrs117124364
SNP Nexus

SNPshotrs117124364
SNPdbers117124364
MSV3drs117124364
GWAS Ctlgrs117124364
GMAF0.005969
Max Magnitude
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Bulimia nervosa
Title Genetic variants associated with disordered eating.
Risk Allele C
P-val 9E-6
Odds Ratio .16 [0.089-0.231] unit decrease