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rs1506203

From SNPedia

Orientationminus
Stabilizedminus
Make rs1506203(A;A)
Make rs1506203(A;C)
Make rs1506203(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position30999011
is asnp
is mentioned by
dbSNPrs1506203
ebirs1506203
HLIrs1506203
Exacrs1506203
Varsomers1506203
Maprs1506203
PheGenIrs1506203
hapmaprs1506203
1000 genomesrs1506203
hgdprs1506203
ensemblrs1506203
gopubmedrs1506203
geneviewrs1506203
scholarrs1506203
googlers1506203
pharmgkbrs1506203
gwascentralrs1506203
openSNPrs1506203
23andMers1506203
23andMe allrs1506203
SNP Nexus

SNPshotrs1506203
SNPdbers1506203
MSV3drs1506203
GWAS Ctlgrs1506203
GMAF0.1933
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Eating disorders (purging via substances)
Title Genetic variants associated with disordered eating.
Risk Allele G
P-val 8E-6
Odds Ratio .08 [0.048-0.118] unit decrease