rs121908591

Orientation

plus

Stabilized

plus

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

Make rs121908591(C;T)

Make rs121908591(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

5045727

Gene

KCNA5

is a	snp
is	mentioned by
dbSNP	rs121908591
dbSNP (classic)	rs121908591
ClinGen	rs121908591
ebi	rs121908591
HLI	rs121908591
Exac	rs121908591
Gnomad	rs121908591
Varsome	rs121908591
LitVar	rs121908591
Map	rs121908591
PheGenI	rs121908591
Biobank	rs121908591
1000 genomes	rs121908591
hgdp	rs121908591
ensembl	rs121908591
geneview	rs121908591
scholar	rs121908591
google	rs121908591
pharmgkb	rs121908591
gwascentral	rs121908591
openSNP	rs121908591
23andMe	rs121908591
SNPshot	rs121908591
SNPdbe	rs121908591
MSV3d	rs121908591
GWAS Ctlg	rs121908591

GMAF

0.001377

Max Magnitude

0

OMIM	176267
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908591(T;T)
Alt	rs121908591(T;T)
Reference	Rs121908591(C;C)
Significance	Pathogenic
Disease	Atrial fibrillation not specified
Variation	info
Gene	KCNA5
CLNDBN	Atrial fibrillation, familial, 7 not specified
Reversed	0
HGVS	NC_000012.11:g.5154893C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014412.18, RCV000295612.1,