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rs6999631

From SNPedia

Orientationplus
Stabilizedplus
Make rs6999631(C;C)
Make rs6999631(C;G)
Make rs6999631(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position10228901
GeneMSRA
is asnp
is mentioned by
dbSNPrs6999631
ebirs6999631
HLIrs6999631
Exacrs6999631
Varsomers6999631
Maprs6999631
PheGenIrs6999631
hapmaprs6999631
1000 genomesrs6999631
hgdprs6999631
ensemblrs6999631
gopubmedrs6999631
geneviewrs6999631
scholarrs6999631
googlers6999631
pharmgkbrs6999631
gwascentralrs6999631
openSNPrs6999631
23andMers6999631
23andMe allrs6999631
SNP Nexus

SNPshotrs6999631
SNPdbers6999631
MSV3drs6999631
GWAS Ctlgrs6999631
GMAF0.1547
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Bulimia nervosa
Title Genetic variants associated with disordered eating.
Risk Allele C
P-val 8E-6
Odds Ratio .09 [0.051-0.129] unit decrease