rs199473073

Orientation

minus

Stabilized

minus

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

Make rs199473073(C;C)

Make rs199473073(C;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38613757

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473073
dbSNP (classic)	rs199473073
ClinGen	rs199473073
ebi	rs199473073
HLI	rs199473073
Exac	rs199473073
Gnomad	rs199473073
Varsome	rs199473073
LitVar	rs199473073
Map	rs199473073
PheGenI	rs199473073
Biobank	rs199473073
1000 genomes	rs199473073
hgdp	rs199473073
ensembl	rs199473073
geneview	rs199473073
scholar	rs199473073
google	rs199473073
pharmgkb	rs199473073
gwascentral	rs199473073
openSNP	rs199473073
23andMe	rs199473073
SNPshot	rs199473073
SNPdbe	rs199473073
MSV3d	rs199473073
GWAS Ctlg	rs199473073

Max Magnitude

0

ClinVar
Risk	rs199473073(C;C)
Alt	rs199473073(C;C)
Reference	Rs199473073(T;T)
Significance	Untested
Disease	Cardiac conduction defect
Variation	info
Gene	SCN5A
CLNDBN	Cardiac conduction defect, nonspecific
Reversed	1
HGVS	NC_000003.11:g.38655248A>G
CLNSRC	ClinVar
CLNACC	RCV000058839.3,