rs199473335

Orientation

minus

Stabilized

minus

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

Make rs199473335(A;A)

Make rs199473335(A;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

38550411

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473335
dbSNP (classic)	rs199473335
ClinGen	rs199473335
ebi	rs199473335
HLI	rs199473335
Exac	rs199473335
Gnomad	rs199473335
Varsome	rs199473335
LitVar	rs199473335
Map	rs199473335
PheGenI	rs199473335
Biobank	rs199473335
1000 genomes	rs199473335
hgdp	rs199473335
ensembl	rs199473335
geneview	rs199473335
scholar	rs199473335
google	rs199473335
pharmgkb	rs199473335
gwascentral	rs199473335
openSNP	rs199473335
23andMe	rs199473335
SNPshot	rs199473335
SNPdbe	rs199473335
MSV3d	rs199473335
GWAS Ctlg	rs199473335

Max Magnitude

0

ClinVar
Risk	rs199473335(A;A)
Alt	rs199473335(A;A)
Reference	Rs199473335(C;C)
Significance	Pathogenic
Disease	Atrial fibrillation Atrial fibrillation not specified
Variation	info
Gene	SCN5A
CLNDBN	Atrial fibrillation, familial, 10 Atrial fibrillation not specified
Reversed	1
HGVS	NC_000003.11:g.38591902G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022947.2, RCV000058818.3, RCV000148858.1, RCV000154830.1,