rs1056468

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs1056468(A;T)

Make rs1056468(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

5046497

Gene

KCNA5

is a	snp
is	mentioned by
dbSNP	rs1056468
dbSNP (classic)	rs1056468
ClinGen	rs1056468
ebi	rs1056468
HLI	rs1056468
Exac	rs1056468
Gnomad	rs1056468
Varsome	rs1056468
LitVar	rs1056468
Map	rs1056468
PheGenI	rs1056468
Biobank	rs1056468
1000 genomes	rs1056468
hgdp	rs1056468
ensembl	rs1056468
geneview	rs1056468
scholar	rs1056468
google	rs1056468
pharmgkb	rs1056468
gwascentral	rs1056468
openSNP	rs1056468
23andMe	rs1056468
SNPshot	rs1056468
SNPdbe	rs1056468
MSV3d	rs1056468
GWAS Ctlg	rs1056468

Max Magnitude

0

?	(A;A) (A;T) (T;T)	28

[PMID 26309673] 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,