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rs199473178

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473178(C;C)
Make rs199473178(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585695
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473178
ebirs199473178
HLIrs199473178
Exacrs199473178
Varsomers199473178
Maprs199473178
PheGenIrs199473178
hapmaprs199473178
1000 genomesrs199473178
hgdprs199473178
ensemblrs199473178
gopubmedrs199473178
geneviewrs199473178
scholarrs199473178
googlers199473178
pharmgkbrs199473178
gwascentralrs199473178
openSNPrs199473178
23andMers199473178
23andMe allrs199473178
SNP Nexus

SNPshotrs199473178
SNPdbers199473178
MSV3drs199473178
GWAS Ctlgrs199473178
Max Magnitude0
ClinVar
Risk rs199473178(C;C)
Alt rs199473178(C;C)
Reference rs199473178(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627186A>G
CLNSRC ClinVar
CLNACC RCV000058527.2,