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

rs199473271

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473271(A;A)
Make rs199473271(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38554450
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473271
ebirs199473271
HLIrs199473271
Exacrs199473271
Varsomers199473271
Maprs199473271
PheGenIrs199473271
hapmaprs199473271
1000 genomesrs199473271
hgdprs199473271
ensemblrs199473271
gopubmedrs199473271
geneviewrs199473271
scholarrs199473271
googlers199473271
pharmgkbrs199473271
gwascentralrs199473271
openSNPrs199473271
23andMers199473271
23andMe allrs199473271
SNP Nexus

SNPshotrs199473271
SNPdbers199473271
MSV3drs199473271
GWAS Ctlgrs199473271
Max Magnitude0
ClinVar
Risk rs199473271(A;A)
Alt rs199473271(A;A)
Reference rs199473271(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38595941C>T
CLNSRC ClinVar
CLNACC RCV000058694.2,