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rs199473302

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473302(C;C)
Make rs199473302(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551190
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473302
ebirs199473302
HLIrs199473302
Exacrs199473302
Varsomers199473302
Maprs199473302
PheGenIrs199473302
hapmaprs199473302
1000 genomesrs199473302
hgdprs199473302
ensemblrs199473302
gopubmedrs199473302
geneviewrs199473302
scholarrs199473302
googlers199473302
pharmgkbrs199473302
gwascentralrs199473302
openSNPrs199473302
23andMers199473302
23andMe allrs199473302
SNP Nexus

SNPshotrs199473302
SNPdbers199473302
MSV3drs199473302
GWAS Ctlgrs199473302
Max Magnitude0
ClinVar
Risk rs199473302(C;C)
Alt rs199473302(C;C)
Reference rs199473302(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592681A>G
CLNSRC ClinVar
CLNACC RCV000058749.2,