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rs114945094

From SNPedia

Orientationplus
Stabilizedplus
Make rs114945094(A;A)
Make rs114945094(A;G)
Make rs114945094(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position12153806
is asnp
is mentioned by
dbSNPrs114945094
dbSNP (old)rs114945094
ClinGenrs114945094
ebirs114945094
HLIrs114945094
Exacrs114945094
Gnomadrs114945094
Varsomers114945094
Maprs114945094
PheGenIrs114945094
Biobankrs114945094
1000 genomesrs114945094
hgdprs114945094
ensemblrs114945094
gopubmedrs114945094
geneviewrs114945094
scholarrs114945094
googlers114945094
pharmgkbrs114945094
gwascentralrs114945094
openSNPrs114945094
23andMers114945094
23andMe allrs114945094
SNP Nexus

SNPshotrs114945094
SNPdbers114945094
MSV3drs114945094
GWAS Ctlgrs114945094
GMAF0.2479
Max Magnitude
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Anorexia nervosa
Title Genetic variants associated with disordered eating.
Risk Allele G
P-val 4E-6
Odds Ratio .14 [0.078-0.192] unit decrease