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rs199473168

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473168(C;T)
Make rs199473168(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585846
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473168
ebirs199473168
HLIrs199473168
Exacrs199473168
Varsomers199473168
Maprs199473168
PheGenIrs199473168
hapmaprs199473168
1000 genomesrs199473168
hgdprs199473168
ensemblrs199473168
gopubmedrs199473168
geneviewrs199473168
scholarrs199473168
googlers199473168
pharmgkbrs199473168
gwascentralrs199473168
openSNPrs199473168
23andMers199473168
23andMe allrs199473168
SNP Nexus

SNPshotrs199473168
SNPdbers199473168
MSV3drs199473168
GWAS Ctlgrs199473168
Max Magnitude0
ClinVar
Risk rs199473168(T;T)
Alt rs199473168(T;T)
Reference rs199473168(C;C)
Significance Pathogenic
Disease Brugada syndrome not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38627337G>A
CLNSRC ClinVar
CLNACC RCV000058513.2, RCV000183008.2,