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rs2537859

From SNPedia

Orientationplus
Stabilizedplus
Make rs2537859(C;C)
Make rs2537859(C;T)
Make rs2537859(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position54616651
is asnp
is mentioned by
dbSNPrs2537859
ebirs2537859
HLIrs2537859
Exacrs2537859
Varsomers2537859
Maprs2537859
PheGenIrs2537859
hapmaprs2537859
1000 genomesrs2537859
hgdprs2537859
ensemblrs2537859
gopubmedrs2537859
geneviewrs2537859
scholarrs2537859
googlers2537859
pharmgkbrs2537859
gwascentralrs2537859
openSNPrs2537859
23andMers2537859
23andMe allrs2537859
SNP Nexus

SNPshotrs2537859
SNPdbers2537859
MSV3drs2537859
GWAS Ctlgrs2537859
GMAF0.4977
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000004
Odds Ratio 1.16 [1.09-1.24]


GET Evidence
rs2537859
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.460317
summary