Rs2314398

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ReferenceGRCh38 38.1/141
Chromosome2
Position96747751
is asnp
is mentioned by
dbSNPrs2314398
Exacrs2314398
PheGenIrs2314398
nextbiors2314398
hapmaprs2314398
1000 genomesrs2314398
hgdprs2314398
ensemblrs2314398
gopubmedrs2314398
geneviewrs2314398
scholarrs2314398
googlers2314398
pharmgkbrs2314398
gwascentralrs2314398
openSNPrs2314398
23andMers2314398
23andMe allrs2314398
SNP Nexus

SNPshotrs2314398
SNPdbers2314398
MSV3drs2314398
GMAF0.2603
? (C;C) (C;G) (G;G) 28
GWAS
SNP rs2314398
PubMedID [PMID 18711365OA-icon.png]
Condition Bipolar disorder
Gene Intergenic
Risk Allele
pValue 3.00E-006
OR 1.17
95% CI



GET Evidence
rs2314398
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary



[PMID 25124521] Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain