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rs199473156

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473156(C;C)
Make rs199473156(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38587545
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473156
ebirs199473156
HLIrs199473156
Exacrs199473156
Varsomers199473156
Maprs199473156
PheGenIrs199473156
hapmaprs199473156
1000 genomesrs199473156
hgdprs199473156
ensemblrs199473156
gopubmedrs199473156
geneviewrs199473156
scholarrs199473156
googlers199473156
pharmgkbrs199473156
gwascentralrs199473156
openSNPrs199473156
23andMers199473156
23andMe allrs199473156
SNP Nexus

SNPshotrs199473156
SNPdbers199473156
MSV3drs199473156
GWAS Ctlgrs199473156
Max Magnitude0
ClinVar
Risk rs199473156(C,G;C,G)
Alt rs199473156(C,G;C,G)
Reference rs199473156(T;T)
Significance Pathogenic
Disease Brugada syndrome not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38629036A>C; NC_000003.11:g.38629036A>G
CLNSRC ClinVar
CLNACC RCV000058494.2, RCV000183000.1,