rs121908592

Orientation

plus

Stabilized

plus

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

Make rs121908592(C;T)

Make rs121908592(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

5045874

Gene

KCNA5

is a	snp
is	mentioned by
dbSNP	rs121908592
dbSNP (classic)	rs121908592
ClinGen	rs121908592
ebi	rs121908592
HLI	rs121908592
Exac	rs121908592
Gnomad	rs121908592
Varsome	rs121908592
LitVar	rs121908592
Map	rs121908592
PheGenI	rs121908592
Biobank	rs121908592
1000 genomes	rs121908592
hgdp	rs121908592
ensembl	rs121908592
geneview	rs121908592
scholar	rs121908592
google	rs121908592
pharmgkb	rs121908592
gwascentral	rs121908592
openSNP	rs121908592
23andMe	rs121908592
SNPshot	rs121908592
SNPdbe	rs121908592
MSV3d	rs121908592
GWAS Ctlg	rs121908592

Max Magnitude

0

OMIM	176267
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121908592(T;T)
Alt	rs121908592(T;T)
Reference	Rs121908592(C;C)
Significance	Pathogenic
Disease	Atrial fibrillation
Variation	info
Gene	KCNA5
CLNDBN	Atrial fibrillation, familial, 7
Reversed	0
HGVS	NC_000012.11:g.5155040C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014413.24,