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rs199473169

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473169(A;C)
Make rs199473169(C;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585821
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473169
ebirs199473169
HLIrs199473169
Exacrs199473169
Varsomers199473169
Maprs199473169
PheGenIrs199473169
hapmaprs199473169
1000 genomesrs199473169
hgdprs199473169
ensemblrs199473169
gopubmedrs199473169
geneviewrs199473169
scholarrs199473169
googlers199473169
pharmgkbrs199473169
gwascentralrs199473169
openSNPrs199473169
23andMers199473169
23andMe allrs199473169
SNP Nexus

SNPshotrs199473169
SNPdbers199473169
MSV3drs199473169
GWAS Ctlgrs199473169
Max Magnitude0
ClinVar
Risk rs199473169(C;C)
Alt rs199473169(C;C)
Reference rs199473169(A;A)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627312T>G
CLNSRC ClinVar
CLNACC RCV000058515.2,