rs199473625

Orientation

minus

Stabilized

minus

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

Make rs199473625(A;G)

Make rs199473625(G;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38551394

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473625
dbSNP (classic)	rs199473625
ClinGen	rs199473625
ebi	rs199473625
HLI	rs199473625
Exac	rs199473625
Gnomad	rs199473625
Varsome	rs199473625
LitVar	rs199473625
Map	rs199473625
PheGenI	rs199473625
Biobank	rs199473625
1000 genomes	rs199473625
hgdp	rs199473625
ensembl	rs199473625
geneview	rs199473625
scholar	rs199473625
google	rs199473625
pharmgkb	rs199473625
gwascentral	rs199473625
openSNP	rs199473625
23andMe	rs199473625
SNPshot	rs199473625
SNPdbe	rs199473625
MSV3d	rs199473625
GWAS Ctlg	rs199473625

Max Magnitude

0

ClinVar
Risk	rs199473625(G;G)
Alt	rs199473625(G;G)
Reference	Rs199473625(A;A)
Significance	Probable-Pathogenic
Disease	Congenital long QT syndrome not provided
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome not provided
Reversed	1
HGVS	NC_000003.11:g.38592885T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058732.3, RCV000183093.4,