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rs199473275

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473275(C;C)
Make rs199473275(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38554347
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473275
ebirs199473275
HLIrs199473275
Exacrs199473275
Varsomers199473275
Maprs199473275
PheGenIrs199473275
hapmaprs199473275
1000 genomesrs199473275
hgdprs199473275
ensemblrs199473275
gopubmedrs199473275
geneviewrs199473275
scholarrs199473275
googlers199473275
pharmgkbrs199473275
gwascentralrs199473275
openSNPrs199473275
23andMers199473275
23andMe allrs199473275
SNP Nexus

SNPshotrs199473275
SNPdbers199473275
MSV3drs199473275
GWAS Ctlgrs199473275
Max Magnitude0
ClinVar
Risk rs199473275(C;C)
Alt rs199473275(C;C)
Reference rs199473275(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38595838A>G
CLNSRC ClinVar
CLNACC RCV000058700.2,