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

rs199473095

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473095(G;T)
Make rs199473095(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606757
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473095
ebirs199473095
HLIrs199473095
Exacrs199473095
Varsomers199473095
Maprs199473095
PheGenIrs199473095
hapmaprs199473095
1000 genomesrs199473095
hgdprs199473095
ensemblrs199473095
gopubmedrs199473095
geneviewrs199473095
scholarrs199473095
googlers199473095
pharmgkbrs199473095
gwascentralrs199473095
openSNPrs199473095
23andMers199473095
23andMe allrs199473095
SNP Nexus

SNPshotrs199473095
SNPdbers199473095
MSV3drs199473095
GWAS Ctlgrs199473095
Max Magnitude0
ClinVar
Risk rs199473095(A,T;A,T)
Alt rs199473095(A,T;A,T)
Reference rs199473095(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38648248C>A; NC_000003.11:g.38648248C>T
CLNSRC ClinVar
CLNACC RCV000058386.2, RCV000058385.2,