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rs74566133

From SNPedia

Orientationplus
Stabilizedplus
Make rs74566133(C;C)
Make rs74566133(C;T)
Make rs74566133(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position133766099
is asnp
is mentioned by
dbSNPrs74566133
ebirs74566133
HLIrs74566133
Exacrs74566133
Varsomers74566133
Maprs74566133
PheGenIrs74566133
hapmaprs74566133
1000 genomesrs74566133
hgdprs74566133
ensemblrs74566133
gopubmedrs74566133
geneviewrs74566133
scholarrs74566133
googlers74566133
pharmgkbrs74566133
gwascentralrs74566133
openSNPrs74566133
23andMers74566133
23andMe allrs74566133
SNP Nexus

SNPshotrs74566133
SNPdbers74566133
MSV3drs74566133
GWAS Ctlgrs74566133
GMAF0.01469
Max Magnitude
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Eating disorders (purging via substances)
Title Genetic variants associated with disordered eating.
Risk Allele C
P-val 7E-7
Odds Ratio .25 [0.15-0.35] unit decrease