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rs199473261

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473261(A;A)
Make rs199473261(A;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38555718
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473261
ebirs199473261
HLIrs199473261
Exacrs199473261
Varsomers199473261
Maprs199473261
PheGenIrs199473261
hapmaprs199473261
1000 genomesrs199473261
hgdprs199473261
ensemblrs199473261
gopubmedrs199473261
geneviewrs199473261
scholarrs199473261
googlers199473261
pharmgkbrs199473261
gwascentralrs199473261
openSNPrs199473261
23andMers199473261
23andMe allrs199473261
SNP Nexus

SNPshotrs199473261
SNPdbers199473261
MSV3drs199473261
GWAS Ctlgrs199473261
Max Magnitude0
ClinVar
Risk rs199473261(A;A)
Alt rs199473261(A;A)
Reference rs199473261(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38597209A>T
CLNSRC ClinVar
CLNACC RCV000058679.2,