rs199473325

Orientation

minus

Stabilized

minus

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

Make rs199473325(A;A)

Make rs199473325(A;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38550671

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473325
dbSNP (classic)	rs199473325
ClinGen	rs199473325
ebi	rs199473325
HLI	rs199473325
Exac	rs199473325
Gnomad	rs199473325
Varsome	rs199473325
LitVar	rs199473325
Map	rs199473325
PheGenI	rs199473325
Biobank	rs199473325
1000 genomes	rs199473325
hgdp	rs199473325
ensembl	rs199473325
geneview	rs199473325
scholar	rs199473325
google	rs199473325
pharmgkb	rs199473325
gwascentral	rs199473325
openSNP	rs199473325
23andMe	rs199473325
SNPshot	rs199473325
SNPdbe	rs199473325
MSV3d	rs199473325
GWAS Ctlg	rs199473325

Max Magnitude

0

ClinVar
Risk	rs199473325(A;A) rs199473325(C;C)
Alt	rs199473325(A;A) rs199473325(C;C)
Reference	Rs199473325(G;G)
Significance	Untested
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.38592162C>G; NC_000003.11:g.38592162C>T
CLNSRC	ClinVar
CLNACC	RCV000058801.3, RCV000058800.3,