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rs199473272

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473272(A;C)
Make rs199473272(C;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38554435
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473272
ebirs199473272
HLIrs199473272
Exacrs199473272
Varsomers199473272
Maprs199473272
PheGenIrs199473272
hapmaprs199473272
1000 genomesrs199473272
hgdprs199473272
ensemblrs199473272
gopubmedrs199473272
geneviewrs199473272
scholarrs199473272
googlers199473272
pharmgkbrs199473272
gwascentralrs199473272
openSNPrs199473272
23andMers199473272
23andMe allrs199473272
SNP Nexus

SNPshotrs199473272
SNPdbers199473272
MSV3drs199473272
GWAS Ctlgrs199473272
Max Magnitude0
ClinVar
Risk rs199473272(C;C)
Alt rs199473272(C;C)
Reference rs199473272(A;A)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38595926T>G
CLNSRC ClinVar
CLNACC RCV000058695.2,