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rs2905072

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2905072(C;C)
Make rs2905072(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position132969648
is asnp
is mentioned by
dbSNPrs2905072
ebirs2905072
HLIrs2905072
Exacrs2905072
Varsomers2905072
Maprs2905072
PheGenIrs2905072
hapmaprs2905072
1000 genomesrs2905072
hgdprs2905072
ensemblrs2905072
gopubmedrs2905072
geneviewrs2905072
scholarrs2905072
googlers2905072
pharmgkbrs2905072
gwascentralrs2905072
openSNPrs2905072
23andMers2905072
23andMe allrs2905072
SNP Nexus

SNPshotrs2905072
SNPdbers2905072
MSV3drs2905072
GWAS Ctlgrs2905072
GMAF0.2185
Max Magnitude0
? (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 A
P-val 0.000006
Odds Ratio 1.21 [1.11-1.32]


GET Evidence
rs2905072
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.789062
summary