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

rs199473586

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473586(C;C)
Make rs199473586(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585927
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473586
ebirs199473586
HLIrs199473586
Exacrs199473586
Varsomers199473586
Maprs199473586
PheGenIrs199473586
hapmaprs199473586
1000 genomesrs199473586
hgdprs199473586
ensemblrs199473586
gopubmedrs199473586
geneviewrs199473586
scholarrs199473586
googlers199473586
pharmgkbrs199473586
gwascentralrs199473586
openSNPrs199473586
23andMers199473586
23andMe allrs199473586
SNP Nexus

SNPshotrs199473586
SNPdbers199473586
MSV3drs199473586
GWAS Ctlgrs199473586
Max Magnitude0
ClinVar
Risk rs199473586(C;C)
Alt rs199473586(C;C)
Reference rs199473586(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627418A>G
CLNSRC ClinVar
CLNACC RCV000058510.2,