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rs199473213

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473213(A;A)
Make rs199473213(A;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38566503
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473213
ebirs199473213
HLIrs199473213
Exacrs199473213
Varsomers199473213
Maprs199473213
PheGenIrs199473213
hapmaprs199473213
1000 genomesrs199473213
hgdprs199473213
ensemblrs199473213
gopubmedrs199473213
geneviewrs199473213
scholarrs199473213
googlers199473213
pharmgkbrs199473213
gwascentralrs199473213
openSNPrs199473213
23andMers199473213
23andMe allrs199473213
SNP Nexus

SNPshotrs199473213
SNPdbers199473213
MSV3drs199473213
GWAS Ctlgrs199473213
Max Magnitude0
ClinVar
Risk rs199473213(A;A)
Alt rs199473213(A;A)
Reference rs199473213(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38607994A>T
CLNSRC ClinVar
CLNACC RCV000058597.2,