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rs587777742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777742(C;T)
Make rs587777742(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position18340958
GeneCACNB2
is asnp
is mentioned by
dbSNPrs587777742
ebirs587777742
HLIrs587777742
Exacrs587777742
Varsomers587777742
Maprs587777742
PheGenIrs587777742
hapmaprs587777742
1000 genomesrs587777742
hgdprs587777742
ensemblrs587777742
gopubmedrs587777742
geneviewrs587777742
scholarrs587777742
googlers587777742
pharmgkbrs587777742
gwascentralrs587777742
openSNPrs587777742
23andMers587777742
23andMe allrs587777742
SNP Nexus

SNPshotrs587777742
SNPdbers587777742
MSV3drs587777742
GWAS Ctlgrs587777742
Max Magnitude0
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,