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rs199473566

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473566(G;G)
Make rs199473566(G;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606689
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473566
ebirs199473566
HLIrs199473566
Exacrs199473566
Varsomers199473566
Maprs199473566
PheGenIrs199473566
hapmaprs199473566
1000 genomesrs199473566
hgdprs199473566
ensemblrs199473566
gopubmedrs199473566
geneviewrs199473566
scholarrs199473566
googlers199473566
pharmgkbrs199473566
gwascentralrs199473566
openSNPrs199473566
23andMers199473566
23andMe allrs199473566
SNP Nexus

SNPshotrs199473566
SNPdbers199473566
MSV3drs199473566
GWAS Ctlgrs199473566
Max Magnitude0
ClinVar
Risk rs199473566(G;G)
Alt rs199473566(G;G)
Reference rs199473566(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38648180A>C
CLNSRC ClinVar
CLNACC RCV000058394.2,