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rs199473269

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473269(A;A)
Make rs199473269(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38554519
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473269
ebirs199473269
HLIrs199473269
Exacrs199473269
Varsomers199473269
Maprs199473269
PheGenIrs199473269
hapmaprs199473269
1000 genomesrs199473269
hgdprs199473269
ensemblrs199473269
gopubmedrs199473269
geneviewrs199473269
scholarrs199473269
googlers199473269
pharmgkbrs199473269
gwascentralrs199473269
openSNPrs199473269
23andMers199473269
23andMe allrs199473269
SNP Nexus

SNPshotrs199473269
SNPdbers199473269
MSV3drs199473269
GWAS Ctlgrs199473269
Max Magnitude0
ClinVar
Risk rs199473269(A;A)
Alt rs199473269(A;A)
Reference rs199473269(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38596010C>T
CLNSRC ClinVar
CLNACC RCV000058691.2,