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rs1056468

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1056468(A;T)
Make rs1056468(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position5046497
GeneKCNA5
is asnp
is mentioned by
dbSNPrs1056468
dbSNP (old)rs1056468
ClinGenrs1056468
ebirs1056468
HLIrs1056468
Exacrs1056468
Gnomadrs1056468
Varsomers1056468
Maprs1056468
PheGenIrs1056468
Biobankrs1056468
1000 genomesrs1056468
hgdprs1056468
ensemblrs1056468
gopubmedrs1056468
geneviewrs1056468
scholarrs1056468
googlers1056468
pharmgkbrs1056468
gwascentralrs1056468
openSNPrs1056468
23andMers1056468
23andMe allrs1056468
SNP Nexus

SNPshotrs1056468
SNPdbers1056468
MSV3drs1056468
GWAS Ctlgrs1056468
Max Magnitude0
? (A;A) (A;T) (T;T) 28
[PMID 26309673OA-icon.png] KCNA5 gene polymorphism associate with idiopathic atrial fibrillation


ClinVar
Risk rs1056468(T;T)
Alt rs1056468(T;T)
Reference Rs1056468(A;A)
Significance Probable-non-pathogenic
Disease Familial atrial fibrillation
Variation info
Gene KCNA5
CLNDBN Familial atrial fibrillation
Reversed 0
HGVS NC_000012.11:g.5155663A>T
CLNSRC
CLNACC RCV000399775.1,