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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
ebirs2242663
HLIrs2242663
Exacrs2242663
Varsomers2242663
Maprs2242663
PheGenIrs2242663
hapmaprs2242663
1000 genomesrs2242663
hgdprs2242663
ensemblrs2242663
gopubmedrs2242663
geneviewrs2242663
scholarrs2242663
googlers2242663
pharmgkbrs2242663
gwascentralrs2242663
openSNPrs2242663
23andMers2242663
23andMe allrs2242663
SNP Nexus

SNPshotrs2242663
SNPdbers2242663
MSV3drs2242663
GWAS Ctlgrs2242663
GMAF0.2456
Max Magnitude
? (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]


GET Evidence
rs2242663
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.148438
summary