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rs199473066

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473066(C;C)
Make rs199473066(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38620910
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473066
ebirs199473066
HLIrs199473066
Exacrs199473066
Varsomers199473066
Maprs199473066
PheGenIrs199473066
hapmaprs199473066
1000 genomesrs199473066
hgdprs199473066
ensemblrs199473066
gopubmedrs199473066
geneviewrs199473066
scholarrs199473066
googlers199473066
pharmgkbrs199473066
gwascentralrs199473066
openSNPrs199473066
23andMers199473066
23andMe allrs199473066
SNP Nexus

SNPshotrs199473066
SNPdbers199473066
MSV3drs199473066
GWAS Ctlgrs199473066
Max Magnitude0
ClinVar
Risk rs199473066(C;C)
Alt rs199473066(C;C)
Reference rs199473066(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38662401A>G
CLNSRC ClinVar
CLNACC RCV000058781.2,