Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473637(A;A)
Make rs199473637(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38550569
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473637
ebirs199473637
HLIrs199473637
Exacrs199473637
Varsomers199473637
Maprs199473637
PheGenIrs199473637
hapmaprs199473637
1000 genomesrs199473637
hgdprs199473637
ensemblrs199473637
gopubmedrs199473637
geneviewrs199473637
scholarrs199473637
googlers199473637
pharmgkbrs199473637
gwascentralrs199473637
openSNPrs199473637
23andMers199473637
23andMe allrs199473637
SNP Nexus

SNPshotrs199473637
SNPdbers199473637
MSV3drs199473637
GWAS Ctlgrs199473637
Max Magnitude0
ClinVar
Risk rs199473637(A;A)
Alt rs199473637(A;A)
Reference rs199473637(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592060C>T
CLNSRC ClinVar
CLNACC RCV000058807.2,