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rs199473309

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473309(G;T)
Make rs199473309(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551082
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473309
ebirs199473309
HLIrs199473309
Exacrs199473309
Varsomers199473309
Maprs199473309
PheGenIrs199473309
hapmaprs199473309
1000 genomesrs199473309
hgdprs199473309
ensemblrs199473309
gopubmedrs199473309
geneviewrs199473309
scholarrs199473309
googlers199473309
pharmgkbrs199473309
gwascentralrs199473309
openSNPrs199473309
23andMers199473309
23andMe allrs199473309
SNP Nexus

SNPshotrs199473309
SNPdbers199473309
MSV3drs199473309
GWAS Ctlgrs199473309
Max Magnitude0
ClinVar
Risk rs199473309(T;T)
Alt rs199473309(T;T)
Reference rs199473309(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592573C>A
CLNSRC ClinVar
CLNACC RCV000058762.2,