rs137854620

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;G)	6	Brugada Syndrome
(G;G)	0	common in clinvar

Make rs137854620(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

38557268

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs137854620
dbSNP (classic)	rs137854620
ClinGen	rs137854620
ebi	rs137854620
HLI	rs137854620
Exac	rs137854620
Gnomad	rs137854620
Varsome	rs137854620
LitVar	rs137854620
Map	rs137854620
PheGenI	rs137854620
Biobank	rs137854620
1000 genomes	rs137854620
hgdp	rs137854620
ensembl	rs137854620
geneview	rs137854620
scholar	rs137854620
google	rs137854620
pharmgkb	rs137854620
gwascentral	rs137854620
openSNP	rs137854620
23andMe	rs137854620
SNPshot	rs137854620
SNPdbe	rs137854620
MSV3d	rs137854620
GWAS Ctlg	rs137854620

Max Magnitude

6

OMIM	600163
Desc
Variant	0036
Related	also

ClinVar
Risk	rs137854620(A;A)
Alt	rs137854620(A;A)
Reference	Rs137854620(G;G)
Significance	Pathogenic
Disease	Brugada syndrome 1
Variation	info
Gene	SCN5A
CLNDBN	Brugada syndrome 1
Reversed	1
HGVS	NC_000003.11:g.38598759C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010006.5,