rs199473255

Orientation

minus

Stabilized

minus

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

Make rs199473255(A;G)

Make rs199473255(G;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38556463

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473255
dbSNP (classic)	rs199473255
ClinGen	rs199473255
ebi	rs199473255
HLI	rs199473255
Exac	rs199473255
Gnomad	rs199473255
Varsome	rs199473255
LitVar	rs199473255
Map	rs199473255
PheGenI	rs199473255
Biobank	rs199473255
1000 genomes	rs199473255
hgdp	rs199473255
ensembl	rs199473255
geneview	rs199473255
scholar	rs199473255
google	rs199473255
pharmgkb	rs199473255
gwascentral	rs199473255
openSNP	rs199473255
23andMe	rs199473255
SNPshot	rs199473255
SNPdbe	rs199473255
MSV3d	rs199473255
GWAS Ctlg	rs199473255

Max Magnitude

0

ClinVar
Risk	rs199473255(G;G)
Alt	rs199473255(G;G)
Reference	Rs199473255(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.38597954T>C
CLNSRC	ClinVar
CLNACC	RCV000058670.3,