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rs218361

From SNPedia

Orientationminus
Stabilizedminus
Make rs218361(C;C)
Make rs218361(C;T)
Make rs218361(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position115098496
is asnp
is mentioned by
dbSNPrs218361
dbSNP (classic)rs218361
ClinGenrs218361
ebirs218361
HLIrs218361
Exacrs218361
Gnomadrs218361
Varsomers218361
LitVarrs218361
Maprs218361
PheGenIrs218361
Biobankrs218361
1000 genomesrs218361
hgdprs218361
ensemblrs218361
geneviewrs218361
scholarrs218361
googlers218361
pharmgkbrs218361
gwascentralrs218361
openSNPrs218361
23andMers218361
SNPshotrs218361
SNPdbers218361
MSV3drs218361
GWAS Ctlgrs218361
GMAF0.489
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 G
P-val 7E-6
Odds Ratio 1.06 [1.03-1.08]