rs184442491

Orientation

plus

Stabilized

plus

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

Make rs184442491(A;A)

Make rs184442491(A;C)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38603888

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs184442491
dbSNP (classic)	rs184442491
ClinGen	rs184442491
ebi	rs184442491
HLI	rs184442491
Exac	rs184442491
Gnomad	rs184442491
Varsome	rs184442491
LitVar	rs184442491
Map	rs184442491
PheGenI	rs184442491
Biobank	rs184442491
1000 genomes	rs184442491
hgdp	rs184442491
ensembl	rs184442491
geneview	rs184442491
scholar	rs184442491
google	rs184442491
pharmgkb	rs184442491
gwascentral	rs184442491
openSNP	rs184442491
23andMe	rs184442491
SNPshot	rs184442491
SNPdbe	rs184442491
MSV3d	rs184442491
GWAS Ctlg	rs184442491

Max Magnitude

0

ClinVar
Risk	rs184442491(A;A)
Alt	rs184442491(A;A)
Reference	Rs184442491(C;C)
Significance	Untested
Disease	Congenital long QT syndrome Long QT syndrome not specified
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome Long QT syndrome not specified
Reversed	0
HGVS	NC_000003.11:g.38645379C>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058446.3, RCV000148854.1, RCV000456073.1,