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rs3761218

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 0
(C;C) 1.3x risk
(C;T) 0 normal
(G;G) 0
(T;T) normal
ReferenceGRCh38 38.1/141
Chromosome20
Position3795528
GeneCDC25B
is asnp
is mentioned by
dbSNPrs3761218
ebirs3761218
HLIrs3761218
Exacrs3761218
Varsomers3761218
Maprs3761218
PheGenIrs3761218
hapmaprs3761218
1000 genomesrs3761218
hgdprs3761218
ensemblrs3761218
gopubmedrs3761218
geneviewrs3761218
scholarrs3761218
googlers3761218
pharmgkbrs3761218
gwascentralrs3761218
openSNPrs3761218
23andMers3761218
23andMe allrs3761218
SNP Nexus

SNPshotrs3761218
SNPdbers3761218
MSV3drs3761218
GWAS Ctlgrs3761218
GMAF0.337
Max Magnitude0
? (C;C) (C;T) (T;T) 28
rs3761218 has been reported in a large study to be associated with bipolar disorder.

The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 0.97 (CI 0.81-1.15), and for homozygotes, 1.31 (CI 1.09-1.57). [PMID 17554300OA-icon.png]

GWAS
SNP rs3761218
PubMedID [PMID 17554300OA-icon.png]
Condition Bipolar disorder
Gene NR
Risk Allele C
pValue 7.00E-006
OR 1.03
95% CI 1.15-1.23



GWAS snp
PMID [PMID 21254220OA-icon.png]
Trait
Title Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.
Risk Allele
P-val 0.000001
Odds Ratio None None

[PMID 19308021OA-icon.png] Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort.


GET Evidence
rs3761218
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.648438
summary