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rs3741930

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3741930(C;T)
Make rs3741930(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position5043981
GeneKCNA5
is asnp
is mentioned by
dbSNPrs3741930
dbSNP (old)rs3741930
ClinGenrs3741930
ebirs3741930
HLIrs3741930
Exacrs3741930
Varsomers3741930
Maprs3741930
PheGenIrs3741930
Biobankrs3741930
1000 genomesrs3741930
hgdprs3741930
ensemblrs3741930
gopubmedrs3741930
geneviewrs3741930
scholarrs3741930
googlers3741930
pharmgkbrs3741930
gwascentralrs3741930
openSNPrs3741930
23andMers3741930
23andMe allrs3741930
SNP Nexus

SNPshotrs3741930
SNPdbers3741930
MSV3drs3741930
GWAS Ctlgrs3741930
GMAF0.5
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20556823] Association of KCNA5 gene polymorphism with systemic sclerosis-associated pulmonary arterial hypertension in the European Caucasian population


[PMID 26309673OA-icon.png] KCNA5 gene polymorphism associate with idiopathic atrial fibrillation


ClinVar
Risk rs3741930(T;T)
Alt rs3741930(T;T)
Reference Rs3741930(C;C)
Significance Probable-non-pathogenic
Disease Familial atrial fibrillation
Variation info
Gene KCNA5
CLNDBN Familial atrial fibrillation
Reversed 0
HGVS NC_000012.11:g.5153147C>T
CLNSRC
CLNACC RCV000364132.1,