rs192113333

Orientation

plus

Stabilized

plus

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

Make rs192113333(C;T)

Make rs192113333(T;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38620901

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs192113333
dbSNP (classic)	rs192113333
ClinGen	rs192113333
ebi	rs192113333
HLI	rs192113333
Exac	rs192113333
Gnomad	rs192113333
Varsome	rs192113333
LitVar	rs192113333
Map	rs192113333
PheGenI	rs192113333
Biobank	rs192113333
1000 genomes	rs192113333
hgdp	rs192113333
ensembl	rs192113333
geneview	rs192113333
scholar	rs192113333
google	rs192113333
pharmgkb	rs192113333
gwascentral	rs192113333
openSNP	rs192113333
23andMe	rs192113333
SNPshot	rs192113333
SNPdbe	rs192113333
MSV3d	rs192113333
GWAS Ctlg	rs192113333

Max Magnitude

0

ClinVar
Risk	rs192113333(T;T)
Alt	rs192113333(T;T)
Reference	Rs192113333(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.38662392C>T
CLNSRC	ClinVar
CLNACC	RCV000058790.3,