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rs794728898

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728898(A;G)
Make rs794728898(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38550826
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728898
ebirs794728898
HLIrs794728898
Exacrs794728898
Varsomers794728898
Maprs794728898
PheGenIrs794728898
hapmaprs794728898
1000 genomesrs794728898
hgdprs794728898
ensemblrs794728898
gopubmedrs794728898
geneviewrs794728898
scholarrs794728898
googlers794728898
pharmgkbrs794728898
gwascentralrs794728898
openSNPrs794728898
23andMers794728898
23andMe allrs794728898
SNP Nexus

SNPshotrs794728898
SNPdbers794728898
MSV3drs794728898
GWAS Ctlgrs794728898
Max Magnitude0
ClinVar
Risk rs794728898(G;G)
Alt rs794728898(G;G)
Reference rs794728898(A;A)
Significance Probable-Pathogenic
Disease not provided Brugada syndrome
Variation info
Gene SCN5A
CLNDBN not provided Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592317T>C
CLNSRC
CLNACC RCV000183126.2, RCV000227611.1,