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rs115694618

From SNPedia

Orientationplus
Stabilizedplus
Make rs115694618(A;A)
Make rs115694618(A;G)
Make rs115694618(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position87154977
is asnp
is mentioned by
dbSNPrs115694618
ebirs115694618
HLIrs115694618
Exacrs115694618
Varsomers115694618
Maprs115694618
PheGenIrs115694618
hapmaprs115694618
1000 genomesrs115694618
hgdprs115694618
ensemblrs115694618
gopubmedrs115694618
geneviewrs115694618
scholarrs115694618
googlers115694618
pharmgkbrs115694618
gwascentralrs115694618
openSNPrs115694618
23andMers115694618
23andMe allrs115694618
SNP Nexus

SNPshotrs115694618
SNPdbers115694618
MSV3drs115694618
GWAS Ctlgrs115694618
GMAF0.009642
Max Magnitude
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Bulimia nervosa
Title Genetic variants associated with disordered eating.
Risk Allele A
P-val 4E-6
Odds Ratio .12 [0.07-0.176] unit decrease