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rs7690467

From SNPedia

Orientationplus
Stabilizedplus
Make rs7690467(C;C)
Make rs7690467(C;T)
Make rs7690467(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position132405240
is asnp
is mentioned by
dbSNPrs7690467
ebirs7690467
HLIrs7690467
Exacrs7690467
Varsomers7690467
Maprs7690467
PheGenIrs7690467
hapmaprs7690467
1000 genomesrs7690467
hgdprs7690467
ensemblrs7690467
gopubmedrs7690467
geneviewrs7690467
scholarrs7690467
googlers7690467
pharmgkbrs7690467
gwascentralrs7690467
openSNPrs7690467
23andMers7690467
23andMe allrs7690467
SNP Nexus

SNPshotrs7690467
SNPdbers7690467
MSV3drs7690467
GWAS Ctlgrs7690467
GMAF0.3714
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22911880OA-icon.png]
Trait Eating disorders
Title Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.
Risk Allele T
P-val 7E-6
Odds Ratio 1.12 [1.07-1.18]