rs199473286

Orientation

minus

Stabilized

minus

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

Make rs199473286(A;A)

Make rs199473286(A;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38551477

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473286
dbSNP (classic)	rs199473286
ClinGen	rs199473286
ebi	rs199473286
HLI	rs199473286
Exac	rs199473286
Gnomad	rs199473286
Varsome	rs199473286
LitVar	rs199473286
Map	rs199473286
PheGenI	rs199473286
Biobank	rs199473286
1000 genomes	rs199473286
hgdp	rs199473286
ensembl	rs199473286
geneview	rs199473286
scholar	rs199473286
google	rs199473286
pharmgkb	rs199473286
gwascentral	rs199473286
openSNP	rs199473286
23andMe	rs199473286
SNPshot	rs199473286
SNPdbe	rs199473286
MSV3d	rs199473286
GWAS Ctlg	rs199473286

Max Magnitude

0

ClinVar
Risk	rs199473286(A;A)
Alt	rs199473286(A;A)
Reference	Rs199473286(G;G)
Significance	Untested
Disease	Cardiac conduction defect
Variation	info
Gene	SCN5A
CLNDBN	Cardiac conduction defect, nonspecific
Reversed	1
HGVS	NC_000003.11:g.38592968C>T
CLNSRC	ClinVar
CLNACC	RCV000058723.3,