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rs199473158

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473158(C;T)
Make rs199473158(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38587519
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473158
ebirs199473158
HLIrs199473158
Exacrs199473158
Varsomers199473158
Maprs199473158
PheGenIrs199473158
hapmaprs199473158
1000 genomesrs199473158
hgdprs199473158
ensemblrs199473158
gopubmedrs199473158
geneviewrs199473158
scholarrs199473158
googlers199473158
pharmgkbrs199473158
gwascentralrs199473158
openSNPrs199473158
23andMers199473158
23andMe allrs199473158
SNP Nexus

SNPshotrs199473158
SNPdbers199473158
MSV3drs199473158
GWAS Ctlgrs199473158
Max Magnitude0
ClinVar
Risk rs199473158(T;T)
Alt rs199473158(T;T)
Reference rs199473158(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38629010G>A
CLNSRC ClinVar
CLNACC RCV000058496.2,