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rs199473067

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473067(C;T)
Make rs199473067(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38620900
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473067
ebirs199473067
HLIrs199473067
Exacrs199473067
Varsomers199473067
Maprs199473067
PheGenIrs199473067
hapmaprs199473067
1000 genomesrs199473067
hgdprs199473067
ensemblrs199473067
gopubmedrs199473067
geneviewrs199473067
scholarrs199473067
googlers199473067
pharmgkbrs199473067
gwascentralrs199473067
openSNPrs199473067
23andMers199473067
23andMe allrs199473067
SNP Nexus

SNPshotrs199473067
SNPdbers199473067
MSV3drs199473067
GWAS Ctlgrs199473067
Max Magnitude0
ClinVar
Risk rs199473067(T;T)
Alt rs199473067(T;T)
Reference rs199473067(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38662391G>A
CLNSRC ClinVar
CLNACC RCV000058792.2,