rs199473057

Orientation

minus

Stabilized

minus

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

Make rs199473057(A;G)

Make rs199473057(G;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38630360

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473057
dbSNP (classic)	rs199473057
ClinGen	rs199473057
ebi	rs199473057
HLI	rs199473057
Exac	rs199473057
Gnomad	rs199473057
Varsome	rs199473057
LitVar	rs199473057
Map	rs199473057
PheGenI	rs199473057
Biobank	rs199473057
1000 genomes	rs199473057
hgdp	rs199473057
ensembl	rs199473057
geneview	rs199473057
scholar	rs199473057
google	rs199473057
pharmgkb	rs199473057
gwascentral	rs199473057
openSNP	rs199473057
23andMe	rs199473057
SNPshot	rs199473057
SNPdbe	rs199473057
MSV3d	rs199473057
GWAS Ctlg	rs199473057

Max Magnitude

0

ClinVar
Risk	rs199473057(G;G)
Alt	rs199473057(G;G)
Reference	Rs199473057(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000003.11:g.38671851T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058572.3,