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rs56156506

From SNPedia

Orientationplus
Stabilizedplus
Make rs56156506(A;A)
Make rs56156506(A;T)
Make rs56156506(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38140399
is asnp
is mentioned by
dbSNPrs56156506
dbSNP (classic)rs56156506
ClinGenrs56156506
ebirs56156506
HLIrs56156506
Exacrs56156506
Gnomadrs56156506
Varsomers56156506
LitVarrs56156506
Maprs56156506
PheGenIrs56156506
Biobankrs56156506
1000 genomesrs56156506
hgdprs56156506
ensemblrs56156506
geneviewrs56156506
scholarrs56156506
googlers56156506
pharmgkbrs56156506
gwascentralrs56156506
openSNPrs56156506
23andMers56156506
SNPshotrs56156506
SNPdbers56156506
MSV3drs56156506
GWAS Ctlgrs56156506
GMAF0.3035
Max Magnitude0
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Anorexia nervosa
Title Genetic variants associated with disordered eating.
Risk Allele A
P-val 1E-6
Odds Ratio .05 [0.031-0.075] unit decrease