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

rs199473104

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473104(C;C)
Make rs199473104(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606103
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473104
ebirs199473104
HLIrs199473104
Exacrs199473104
Varsomers199473104
Maprs199473104
PheGenIrs199473104
hapmaprs199473104
1000 genomesrs199473104
hgdprs199473104
ensemblrs199473104
gopubmedrs199473104
geneviewrs199473104
scholarrs199473104
googlers199473104
pharmgkbrs199473104
gwascentralrs199473104
openSNPrs199473104
23andMers199473104
23andMe allrs199473104
SNP Nexus

SNPshotrs199473104
SNPdbers199473104
MSV3drs199473104
GWAS Ctlgrs199473104
Max Magnitude0
ClinVar
Risk rs199473104(C;C)
Alt rs199473104(C;C)
Reference rs199473104(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38647594C>G
CLNSRC ClinVar
CLNACC RCV000058399.2,