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rs748312802

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs748312802(C;T)
Make rs748312802(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38560260
GeneSCN5A
is asnp
is mentioned by
dbSNPrs748312802
ebirs748312802
HLIrs748312802
Exacrs748312802
Varsomers748312802
Maprs748312802
PheGenIrs748312802
hapmaprs748312802
1000 genomesrs748312802
hgdprs748312802
ensemblrs748312802
gopubmedrs748312802
geneviewrs748312802
scholarrs748312802
googlers748312802
pharmgkbrs748312802
gwascentralrs748312802
openSNPrs748312802
23andMers748312802
23andMe allrs748312802
SNP Nexus

SNPshotrs748312802
SNPdbers748312802
MSV3drs748312802
GWAS Ctlgrs748312802
Max Magnitude0
ClinVar
Risk rs748312802(T;T)
Alt rs748312802(T;T)
Reference rs748312802(C;C)
Significance Probable-Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 0
HGVS NC_000003.11:g.38601751C>T
CLNSRC
CLNACC RCV000208068.1,