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rs2989476

From SNPedia

Orientationminus
Stabilizedminus
Make rs2989476(C;C)
Make rs2989476(C;G)
Make rs2989476(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position60593587
is asnp
is mentioned by
dbSNPrs2989476
ebirs2989476
HLIrs2989476
Exacrs2989476
Varsomers2989476
Maprs2989476
PheGenIrs2989476
hapmaprs2989476
1000 genomesrs2989476
hgdprs2989476
ensemblrs2989476
gopubmedrs2989476
geneviewrs2989476
scholarrs2989476
googlers2989476
pharmgkbrs2989476
gwascentralrs2989476
openSNPrs2989476
23andMers2989476
23andMe allrs2989476
SNP Nexus

SNPshotrs2989476
SNPdbers2989476
MSV3drs2989476
GWAS Ctlgrs2989476
GMAF0.4844
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21738484OA-icon.png]
Trait
Title Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.
Risk Allele C
P-val 0.000003
Odds Ratio 1.1600 [NR]
GWAS snp
PMID [PMID 21254220OA-icon.png]
Trait
Title Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.
Risk Allele
P-val 0.000002
Odds Ratio None None

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

[PMID 19416921OA-icon.png] Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.