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rs2242663

From SNPedia

Orientationminus
Stabilizedminus
Make rs2242663(A;A)
Make rs2242663(A;G)
Make rs2242663(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position66567837
GeneCTSF
is asnp
is mentioned by
dbSNPrs2242663
dbSNP (classic)rs2242663
ClinGenrs2242663
ebirs2242663
HLIrs2242663
Exacrs2242663
Gnomadrs2242663
Varsomers2242663
LitVarrs2242663
Maprs2242663
PheGenIrs2242663
Biobankrs2242663
1000 genomesrs2242663
hgdprs2242663
ensemblrs2242663
geneviewrs2242663
scholarrs2242663
googlers2242663
pharmgkbrs2242663
gwascentralrs2242663
openSNPrs2242663
23andMers2242663
SNPshotrs2242663
SNPdbers2242663
MSV3drs2242663
GWAS Ctlgrs2242663
GMAF0.2456
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 19416921OA-icon.png]
Trait Bipolar disorder
Title Genome-wide association and meta-analysis of

bipolar disorder in individuals of European ancestry

Risk Allele T
P-val 0.000001
Odds Ratio 1.20 [1.11-1.29]