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

rs199473229

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473229(C;C)
Make rs199473229(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38560361
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473229
ebirs199473229
HLIrs199473229
Exacrs199473229
Varsomers199473229
Maprs199473229
PheGenIrs199473229
hapmaprs199473229
1000 genomesrs199473229
hgdprs199473229
ensemblrs199473229
gopubmedrs199473229
geneviewrs199473229
scholarrs199473229
googlers199473229
pharmgkbrs199473229
gwascentralrs199473229
openSNPrs199473229
23andMers199473229
23andMe allrs199473229
SNP Nexus

SNPshotrs199473229
SNPdbers199473229
MSV3drs199473229
GWAS Ctlgrs199473229
Max Magnitude0
ClinVar
Risk rs199473229(C;C)
Alt rs199473229(C;C)
Reference rs199473229(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38601852A>G
CLNSRC ClinVar
CLNACC RCV000058630.2,