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

rs199473164

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473164(C;C)
Make rs199473164(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585962
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473164
ebirs199473164
HLIrs199473164
Exacrs199473164
Varsomers199473164
Maprs199473164
PheGenIrs199473164
hapmaprs199473164
1000 genomesrs199473164
hgdprs199473164
ensemblrs199473164
gopubmedrs199473164
geneviewrs199473164
scholarrs199473164
googlers199473164
pharmgkbrs199473164
gwascentralrs199473164
openSNPrs199473164
23andMers199473164
23andMe allrs199473164
SNP Nexus

SNPshotrs199473164
SNPdbers199473164
MSV3drs199473164
GWAS Ctlgrs199473164
Max Magnitude0
ClinVar
Risk rs199473164(C;C)
Alt rs199473164(C;C)
Reference rs199473164(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627453A>G
CLNSRC ClinVar
CLNACC RCV000058506.2,