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rs199473236

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473236(G;G)
Make rs199473236(G;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38560313
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473236
ebirs199473236
HLIrs199473236
Exacrs199473236
Varsomers199473236
Maprs199473236
PheGenIrs199473236
hapmaprs199473236
1000 genomesrs199473236
hgdprs199473236
ensemblrs199473236
gopubmedrs199473236
geneviewrs199473236
scholarrs199473236
googlers199473236
pharmgkbrs199473236
gwascentralrs199473236
openSNPrs199473236
23andMers199473236
23andMe allrs199473236
SNP Nexus

SNPshotrs199473236
SNPdbers199473236
MSV3drs199473236
GWAS Ctlgrs199473236
Max Magnitude0
ClinVar
Risk rs199473236(G;G)
Alt rs199473236(G;G)
Reference rs199473236(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38601804A>C
CLNSRC ClinVar
CLNACC RCV000058639.2,