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rs199473179

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473179(C;C)
Make rs199473179(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38581355
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473179
ebirs199473179
HLIrs199473179
Exacrs199473179
Varsomers199473179
Maprs199473179
PheGenIrs199473179
hapmaprs199473179
1000 genomesrs199473179
hgdprs199473179
ensemblrs199473179
gopubmedrs199473179
geneviewrs199473179
scholarrs199473179
googlers199473179
pharmgkbrs199473179
gwascentralrs199473179
openSNPrs199473179
23andMers199473179
23andMe allrs199473179
SNP Nexus

SNPshotrs199473179
SNPdbers199473179
MSV3drs199473179
GWAS Ctlgrs199473179
Max Magnitude0
ClinVar
Risk rs199473179(C;C)
Alt rs199473179(C;C)
Reference rs199473179(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38622846A>G
CLNSRC ClinVar
CLNACC RCV000058529.2,