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

rs199473091

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473091(A;A)
Make rs199473091(A;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38608190
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473091
ebirs199473091
HLIrs199473091
Exacrs199473091
Varsomers199473091
Maprs199473091
PheGenIrs199473091
hapmaprs199473091
1000 genomesrs199473091
hgdprs199473091
ensemblrs199473091
gopubmedrs199473091
geneviewrs199473091
scholarrs199473091
googlers199473091
pharmgkbrs199473091
gwascentralrs199473091
openSNPrs199473091
23andMers199473091
23andMe allrs199473091
SNP Nexus

SNPshotrs199473091
SNPdbers199473091
MSV3drs199473091
GWAS Ctlgrs199473091
Max Magnitude0
ClinVar
Risk rs199473091(A;A)
Alt rs199473091(A;A)
Reference rs199473091(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38649681G>T
CLNSRC ClinVar
CLNACC RCV000058865.2,