rs121908593

Orientation

plus

Stabilized

plus

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

Make rs121908593(A;A)

Make rs121908593(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

5045975

Gene

KCNA5

is a	snp
is	mentioned by
dbSNP	rs121908593
dbSNP (classic)	rs121908593
ClinGen	rs121908593
ebi	rs121908593
HLI	rs121908593
Exac	rs121908593
Gnomad	rs121908593
Varsome	rs121908593
LitVar	rs121908593
Map	rs121908593
PheGenI	rs121908593
Biobank	rs121908593
1000 genomes	rs121908593
hgdp	rs121908593
ensembl	rs121908593
geneview	rs121908593
scholar	rs121908593
google	rs121908593
pharmgkb	rs121908593
gwascentral	rs121908593
openSNP	rs121908593
23andMe	rs121908593
SNPshot	rs121908593
SNPdbe	rs121908593
MSV3d	rs121908593
GWAS Ctlg	rs121908593

Max Magnitude

0

OMIM	176267
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121908593(A;A)
Alt	rs121908593(A;A)
Reference	Rs121908593(G;G)
Significance	Pathogenic
Disease	Atrial fibrillation
Variation	info
Gene	KCNA5
CLNDBN	Atrial fibrillation, familial, 7
Reversed	0
HGVS	NC_000012.11:g.5155141G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014414.26,