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rs28363394

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28363394(C;T)
Make rs28363394(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position138812250
GeneCTNNA1
is asnp
is mentioned by
dbSNPrs28363394
dbSNP (old)rs28363394
ClinGenrs28363394
ebirs28363394
HLIrs28363394
Exacrs28363394
Gnomadrs28363394
Varsomers28363394
Maprs28363394
PheGenIrs28363394
Biobankrs28363394
1000 genomesrs28363394
hgdprs28363394
ensemblrs28363394
gopubmedrs28363394
geneviewrs28363394
scholarrs28363394
googlers28363394
pharmgkbrs28363394
gwascentralrs28363394
openSNPrs28363394
23andMers28363394
23andMe allrs28363394
SNP Nexus

SNPshotrs28363394
SNPdbers28363394
MSV3drs28363394
GWAS Ctlgrs28363394
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 27120077OA-icon.png] Exome Sequencing of Familial Bipolar Disorder. The minor allele of this SNP is one of 84 rare variants speculated to have an impact (positive or negative; see publication for specific SNP details) on risk for bipolar disorder. The analysis of many more patients is likely to be required to confirm or refute this association.


ClinVar
Risk rs28363394(T;T)
Alt rs28363394(T;T)
Reference Rs28363394(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene CTNNA1
CLNDBN not specified
Reversed 0
HGVS NC_000005.9:g.138147939C>T
CLNSRC
CLNACC RCV000465647.1,