rs199473260

Orientation

minus

Stabilized

minus

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

Make rs199473260(A;G)

Make rs199473260(G;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38555720

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473260
dbSNP (classic)	rs199473260
ClinGen	rs199473260
ebi	rs199473260
HLI	rs199473260
Exac	rs199473260
Gnomad	rs199473260
Varsome	rs199473260
LitVar	rs199473260
Map	rs199473260
PheGenI	rs199473260
Biobank	rs199473260
1000 genomes	rs199473260
hgdp	rs199473260
ensembl	rs199473260
geneview	rs199473260
scholar	rs199473260
google	rs199473260
pharmgkb	rs199473260
gwascentral	rs199473260
openSNP	rs199473260
23andMe	rs199473260
SNPshot	rs199473260
SNPdbe	rs199473260
MSV3d	rs199473260
GWAS Ctlg	rs199473260

Max Magnitude

0

ClinVar
Risk	rs199473260(G;G)
Alt	rs199473260(G;G)
Reference	Rs199473260(A;A)
Significance	Probable-Pathogenic
Disease	Congenital long QT syndrome Atrial fibrillation
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome Atrial fibrillation
Reversed	1
HGVS	NC_000003.11:g.38597211T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058678.3, RCV000171569.1,