rs587777742

Orientation

plus

Stabilized

plus

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

Make rs587777742(C;T)

Make rs587777742(T;T)

Reference

GRCh38 38.1/142

Chromosome

10

Position

18340958

Gene

CACNB2

is a	snp
is	mentioned by
dbSNP	rs587777742
dbSNP (classic)	rs587777742
ClinGen	rs587777742
ebi	rs587777742
HLI	rs587777742
Exac	rs587777742
Gnomad	rs587777742
Varsome	rs587777742
LitVar	rs587777742
Map	rs587777742
PheGenI	rs587777742
Biobank	rs587777742
1000 genomes	rs587777742
hgdp	rs587777742
ensembl	rs587777742
geneview	rs587777742
scholar	rs587777742
google	rs587777742
pharmgkb	rs587777742
gwascentral	rs587777742
openSNP	rs587777742
23andMe	rs587777742
SNPshot	rs587777742
SNPdbe	rs587777742
MSV3d	rs587777742
GWAS Ctlg	rs587777742

Max Magnitude

0

ClinVar
Risk	rs587777742(T;T)
Alt	rs587777742(T;T)
Reference	Rs587777742(C;C)
Significance	Pathogenic
Disease	Brugada syndrome 4
Variation	info
Gene	CACNB2
CLNDBN	Brugada syndrome 4
Reversed	0
HGVS	NC_000010.10:g.18629887C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144246.4,