rs199473181

Orientation

minus

Stabilized

minus

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

Make rs199473181(G;T)

Make rs199473181(T;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38581265

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473181
dbSNP (classic)	rs199473181
ClinGen	rs199473181
ebi	rs199473181
HLI	rs199473181
Exac	rs199473181
Gnomad	rs199473181
Varsome	rs199473181
LitVar	rs199473181
Map	rs199473181
PheGenI	rs199473181
Biobank	rs199473181
1000 genomes	rs199473181
hgdp	rs199473181
ensembl	rs199473181
geneview	rs199473181
scholar	rs199473181
google	rs199473181
pharmgkb	rs199473181
gwascentral	rs199473181
openSNP	rs199473181
23andMe	rs199473181
SNPshot	rs199473181
SNPdbe	rs199473181
MSV3d	rs199473181
GWAS Ctlg	rs199473181

Max Magnitude

0

ClinVar
Risk	rs199473181(A;A) rs199473181(T;T)
Alt	rs199473181(A;A) rs199473181(T;T)
Reference	Rs199473181(G;G)
Significance	Untested
Disease	Congenital long QT syndrome Brugada syndrome not specified
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome Brugada syndrome not specified
Reversed	1
HGVS	NC_000003.11:g.38622756C>A; NC_000003.11:g.38622756C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058535.3, RCV000058534.2, RCV000455768.1,