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rs199473194

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473194(C;T)
Make rs199473194(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38579386
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473194
ebirs199473194
HLIrs199473194
Exacrs199473194
Varsomers199473194
Maprs199473194
PheGenIrs199473194
hapmaprs199473194
1000 genomesrs199473194
hgdprs199473194
ensemblrs199473194
gopubmedrs199473194
geneviewrs199473194
scholarrs199473194
googlers199473194
pharmgkbrs199473194
gwascentralrs199473194
openSNPrs199473194
23andMers199473194
23andMe allrs199473194
SNP Nexus

SNPshotrs199473194
SNPdbers199473194
MSV3drs199473194
GWAS Ctlgrs199473194
Max Magnitude0
ClinVar
Risk rs199473194(T;T)
Alt rs199473194(T;T)
Reference rs199473194(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38620877G>A
CLNSRC ClinVar
CLNACC RCV000058565.2,