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

rs199473167

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473167(C;C)
Make rs199473167(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585879
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473167
ebirs199473167
HLIrs199473167
Exacrs199473167
Varsomers199473167
Maprs199473167
PheGenIrs199473167
hapmaprs199473167
1000 genomesrs199473167
hgdprs199473167
ensemblrs199473167
gopubmedrs199473167
geneviewrs199473167
scholarrs199473167
googlers199473167
pharmgkbrs199473167
gwascentralrs199473167
openSNPrs199473167
23andMers199473167
23andMe allrs199473167
SNP Nexus

SNPshotrs199473167
SNPdbers199473167
MSV3drs199473167
GWAS Ctlgrs199473167
Max Magnitude0
ClinVar
Risk rs199473167(C;C)
Alt rs199473167(C;C)
Reference rs199473167(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627370C>G
CLNSRC ClinVar
CLNACC RCV000058512.2,