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rs199473219

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473219(C;C)
Make rs199473219(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38562446
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473219
ebirs199473219
HLIrs199473219
Exacrs199473219
Varsomers199473219
Maprs199473219
PheGenIrs199473219
hapmaprs199473219
1000 genomesrs199473219
hgdprs199473219
ensemblrs199473219
gopubmedrs199473219
geneviewrs199473219
scholarrs199473219
googlers199473219
pharmgkbrs199473219
gwascentralrs199473219
openSNPrs199473219
23andMers199473219
23andMe allrs199473219
SNP Nexus

SNPshotrs199473219
SNPdbers199473219
MSV3drs199473219
GWAS Ctlgrs199473219
Max Magnitude0
ClinVar
Risk rs199473219(C;C)
Alt rs199473219(C;C)
Reference rs199473219(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38603937A>G
CLNSRC ClinVar
CLNACC RCV000058615.2,