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

rs199473559

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473559(C;T)
Make rs199473559(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38620843
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473559
ebirs199473559
HLIrs199473559
Exacrs199473559
Varsomers199473559
Maprs199473559
PheGenIrs199473559
hapmaprs199473559
1000 genomesrs199473559
hgdprs199473559
ensemblrs199473559
gopubmedrs199473559
geneviewrs199473559
scholarrs199473559
googlers199473559
pharmgkbrs199473559
gwascentralrs199473559
openSNPrs199473559
23andMers199473559
23andMe allrs199473559
SNP Nexus

SNPshotrs199473559
SNPdbers199473559
MSV3drs199473559
GWAS Ctlgrs199473559
Max Magnitude0
ClinVar
Risk rs199473559(A,T;A,T)
Alt rs199473559(A,T;A,T)
Reference rs199473559(C;C)
Significance Pathogenic
Disease Brugada syndrome not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38662334G>A; NC_000003.11:g.38662334G>T
CLNSRC ClinVar
CLNACC RCV000058828.2, RCV000182935.2,