rs199794307

Orientation

plus

Stabilized

plus

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

Make rs199794307(A;A)

Make rs199794307(A;G)

Reference

GRCh38 38.1/142

Chromosome

12

Position

5045060

Gene

KCNA5

is a	snp
is	mentioned by
dbSNP	rs199794307
dbSNP (classic)	rs199794307
ClinGen	rs199794307
ebi	rs199794307
HLI	rs199794307
Exac	rs199794307
Gnomad	rs199794307
Varsome	rs199794307
LitVar	rs199794307
Map	rs199794307
PheGenI	rs199794307
Biobank	rs199794307
1000 genomes	rs199794307
hgdp	rs199794307
ensembl	rs199794307
geneview	rs199794307
scholar	rs199794307
google	rs199794307
pharmgkb	rs199794307
gwascentral	rs199794307
openSNP	rs199794307
23andMe	rs199794307
SNPshot	rs199794307
SNPdbe	rs199794307
MSV3d	rs199794307
GWAS Ctlg	rs199794307

Max Magnitude

0

ClinVar
Risk	rs199794307(A;A)
Alt	rs199794307(A;A)
Reference	Rs199794307(G;G)
Significance	Pathogenic
Disease	Atrial fibrillation not provided
Variation	info
Gene	KCNA5
CLNDBN	Atrial fibrillation, familial, 7 not provided
Reversed	0
HGVS	NC_000012.11:g.5154226G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000114990.3, RCV000171655.1,