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rs199473237

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473237(A;A)
Make rs199473237(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38560304
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473237
ebirs199473237
HLIrs199473237
Exacrs199473237
Varsomers199473237
Maprs199473237
PheGenIrs199473237
hapmaprs199473237
1000 genomesrs199473237
hgdprs199473237
ensemblrs199473237
gopubmedrs199473237
geneviewrs199473237
scholarrs199473237
googlers199473237
pharmgkbrs199473237
gwascentralrs199473237
openSNPrs199473237
23andMers199473237
23andMe allrs199473237
SNP Nexus

SNPshotrs199473237
SNPdbers199473237
MSV3drs199473237
GWAS Ctlgrs199473237
Max Magnitude0
ClinVar
Risk rs199473237(A;A)
Alt rs199473237(A;A)
Reference rs199473237(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38601795C>T
CLNSRC ClinVar
CLNACC RCV000058641.2,