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rs199473332

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473332(C;T)
Make rs199473332(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38550481
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473332
ebirs199473332
HLIrs199473332
Exacrs199473332
Varsomers199473332
Maprs199473332
PheGenIrs199473332
hapmaprs199473332
1000 genomesrs199473332
hgdprs199473332
ensemblrs199473332
gopubmedrs199473332
geneviewrs199473332
scholarrs199473332
googlers199473332
pharmgkbrs199473332
gwascentralrs199473332
openSNPrs199473332
23andMers199473332
23andMe allrs199473332
SNP Nexus

SNPshotrs199473332
SNPdbers199473332
MSV3drs199473332
GWAS Ctlgrs199473332
Max Magnitude0
ClinVar
Risk rs199473332(T;T)
Alt rs199473332(T;T)
Reference rs199473332(C;C)
Significance Probable-Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38591972G>A
CLNSRC ClinVar
CLNACC RCV000058814.2,