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rs1557305

From SNPedia

Orientationplus
Stabilizedplus
Make rs1557305(C;C)
Make rs1557305(C;T)
Make rs1557305(T;T)
ReferenceGRCh37.p5 37.3/137
Chromosome18
Position4721359
is asnp
is mentioned by
dbSNPrs1557305
dbSNP (classic)rs1557305
ClinGenrs1557305
ebirs1557305
HLIrs1557305
Exacrs1557305
Gnomadrs1557305
Varsomers1557305
LitVarrs1557305
Maprs1557305
PheGenIrs1557305
Biobankrs1557305
1000 genomesrs1557305
hgdprs1557305
ensemblrs1557305
geneviewrs1557305
scholarrs1557305
googlers1557305
pharmgkbrs1557305
gwascentralrs1557305
openSNPrs1557305
23andMers1557305
SNPshotrs1557305
SNPdbers1557305
MSV3drs1557305
GWAS Ctlgrs1557305
GMAF0.3889
Max Magnitude0
? (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 C
P-val 5E-6
Odds Ratio 1.11 [1.06-1.16]