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rs878855296

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855296(A;A)
Make rs878855296(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position38613790
GeneSCN5A
is asnp
is mentioned by
dbSNPrs878855296
ebirs878855296
HLIrs878855296
Exacrs878855296
Varsomers878855296
Maprs878855296
PheGenIrs878855296
hapmaprs878855296
1000 genomesrs878855296
hgdprs878855296
ensemblrs878855296
gopubmedrs878855296
geneviewrs878855296
scholarrs878855296
googlers878855296
pharmgkbrs878855296
gwascentralrs878855296
openSNPrs878855296
23andMers878855296
23andMe allrs878855296
SNP Nexus

SNPshotrs878855296
SNPdbers878855296
MSV3drs878855296
GWAS Ctlgrs878855296
Max Magnitude0
ClinVar
Risk rs878855296(A;A)
Alt rs878855296(A;A)
Reference rs878855296(G;G)
Significance Probable-Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38655281C>T
CLNSRC
CLNACC RCV000226209.1,