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rs6990255

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs6990255(C;T)
Make rs6990255(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position34269430
is asnp
is mentioned by
dbSNPrs6990255
ebirs6990255
HLIrs6990255
Exacrs6990255
Varsomers6990255
Maprs6990255
PheGenIrs6990255
hapmaprs6990255
1000 genomesrs6990255
hgdprs6990255
ensemblrs6990255
gopubmedrs6990255
geneviewrs6990255
scholarrs6990255
googlers6990255
pharmgkbrs6990255
gwascentralrs6990255
openSNPrs6990255
23andMers6990255
23andMe allrs6990255
SNP Nexus

SNPshotrs6990255
SNPdbers6990255
MSV3drs6990255
GWAS Ctlgrs6990255
GMAF0.09183
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 T
P-val 0.000006
Odds Ratio 1.33 [1.18-1.51]


GET Evidence
rs6990255
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.114035
summary



GWAS snp
PMID [PMID 23453885OA-icon.png]
Trait Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
Title Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Risk Allele T
P-val 2E-6
Odds Ratio 1.15 [1.09-1.20]