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

rs199473611

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473611(C;C)
Make rs199473611(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38557272
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473611
ebirs199473611
HLIrs199473611
Exacrs199473611
Varsomers199473611
Maprs199473611
PheGenIrs199473611
hapmaprs199473611
1000 genomesrs199473611
hgdprs199473611
ensemblrs199473611
gopubmedrs199473611
geneviewrs199473611
scholarrs199473611
googlers199473611
pharmgkbrs199473611
gwascentralrs199473611
openSNPrs199473611
23andMers199473611
23andMe allrs199473611
SNP Nexus

SNPshotrs199473611
SNPdbers199473611
MSV3drs199473611
GWAS Ctlgrs199473611
Max Magnitude0
ClinVar
Risk rs199473611(C;C)
Alt rs199473611(C;C)
Reference rs199473611(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38598763C>G
CLNSRC ClinVar
CLNACC RCV000058653.2,