rs199473075

Orientation

minus

Stabilized

minus

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

Make rs199473075(A;G)

Make rs199473075(G;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38609953

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473075
dbSNP (classic)	rs199473075
ClinGen	rs199473075
ebi	rs199473075
HLI	rs199473075
Exac	rs199473075
Gnomad	rs199473075
Varsome	rs199473075
LitVar	rs199473075
Map	rs199473075
PheGenI	rs199473075
Biobank	rs199473075
1000 genomes	rs199473075
hgdp	rs199473075
ensembl	rs199473075
geneview	rs199473075
scholar	rs199473075
google	rs199473075
pharmgkb	rs199473075
gwascentral	rs199473075
openSNP	rs199473075
23andMe	rs199473075
SNPshot	rs199473075
SNPdbe	rs199473075
MSV3d	rs199473075
GWAS Ctlg	rs199473075

Max Magnitude

0

ClinVar
Risk	rs199473075(G;G)
Alt	rs199473075(G;G)
Reference	Rs199473075(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.38651444T>C
CLNSRC	ClinVar
CLNACC	RCV000058841.3,