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rs2115200

From SNPedia

Orientationminus
Stabilizedminus
Make rs2115200(A;A)
Make rs2115200(A;C)
Make rs2115200(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position39149922
is asnp
is mentioned by
dbSNPrs2115200
dbSNP (classic)rs2115200
ClinGenrs2115200
ebirs2115200
HLIrs2115200
Exacrs2115200
Gnomadrs2115200
Varsomers2115200
LitVarrs2115200
Maprs2115200
PheGenIrs2115200
Biobankrs2115200
1000 genomesrs2115200
hgdprs2115200
ensemblrs2115200
geneviewrs2115200
scholarrs2115200
googlers2115200
pharmgkbrs2115200
gwascentralrs2115200
openSNPrs2115200
23andMers2115200
SNPshotrs2115200
SNPdbers2115200
MSV3drs2115200
GWAS Ctlgrs2115200
GMAF0.1455
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Eating disorders
Title Genetic variants associated with disordered eating.
Risk Allele T
P-val 2E-6
Odds Ratio .10 [0.057-0.139] unit increase