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

rs199473221

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473221(G;G)
Make rs199473221(G;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38560424
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473221
ebirs199473221
HLIrs199473221
Exacrs199473221
Varsomers199473221
Maprs199473221
PheGenIrs199473221
hapmaprs199473221
1000 genomesrs199473221
hgdprs199473221
ensemblrs199473221
gopubmedrs199473221
geneviewrs199473221
scholarrs199473221
googlers199473221
pharmgkbrs199473221
gwascentralrs199473221
openSNPrs199473221
23andMers199473221
23andMe allrs199473221
SNP Nexus

SNPshotrs199473221
SNPdbers199473221
MSV3drs199473221
GWAS Ctlgrs199473221
Max Magnitude0
ClinVar
Risk rs199473221(G;G)
Alt rs199473221(G;G)
Reference rs199473221(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38601915A>C
CLNSRC ClinVar
CLNACC RCV000058617.2,