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rs794728852

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728852(A;A)
Make rs794728852(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38609848
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728852
ebirs794728852
HLIrs794728852
Exacrs794728852
Varsomers794728852
Maprs794728852
PheGenIrs794728852
hapmaprs794728852
1000 genomesrs794728852
hgdprs794728852
ensemblrs794728852
gopubmedrs794728852
geneviewrs794728852
scholarrs794728852
googlers794728852
pharmgkbrs794728852
gwascentralrs794728852
openSNPrs794728852
23andMers794728852
23andMe allrs794728852
SNP Nexus

SNPshotrs794728852
SNPdbers794728852
MSV3drs794728852
GWAS Ctlgrs794728852
Max Magnitude0
ClinVar
Risk rs794728852(A;A)
Alt rs794728852(A;A)
Reference rs794728852(G;G)
Significance Probable-Pathogenic
Disease not specified Brugada syndrome
Variation info
Gene SCN5A
CLNDBN not specified Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38651339C>T
CLNSRC
CLNACC RCV000182948.2, RCV000199539.1,