rs191009474

Orientation

plus

Stabilized

plus

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

Make rs191009474(A;A)

Make rs191009474(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

38606790

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs191009474
dbSNP (classic)	rs191009474
ClinGen	rs191009474
ebi	rs191009474
HLI	rs191009474
Exac	rs191009474
Gnomad	rs191009474
Varsome	rs191009474
LitVar	rs191009474
Map	rs191009474
PheGenI	rs191009474
Biobank	rs191009474
1000 genomes	rs191009474
hgdp	rs191009474
ensembl	rs191009474
geneview	rs191009474
scholar	rs191009474
google	rs191009474
pharmgkb	rs191009474
gwascentral	rs191009474
openSNP	rs191009474
23andMe	rs191009474
SNPshot	rs191009474
SNPdbe	rs191009474
MSV3d	rs191009474
GWAS Ctlg	rs191009474

Max Magnitude

0

ClinVar
Risk	rs191009474(A;A) rs191009474(T;T)
Alt	rs191009474(A;A) rs191009474(T;T)
Reference	Rs191009474(C;C)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000003.11:g.38648281C>T
CLNSRC	ClinVar
CLNACC	RCV000058382.3,