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rs199473211

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473211(C;C)
Make rs199473211(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38566531
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473211
ebirs199473211
HLIrs199473211
Exacrs199473211
Varsomers199473211
Maprs199473211
PheGenIrs199473211
hapmaprs199473211
1000 genomesrs199473211
hgdprs199473211
ensemblrs199473211
gopubmedrs199473211
geneviewrs199473211
scholarrs199473211
googlers199473211
pharmgkbrs199473211
gwascentralrs199473211
openSNPrs199473211
23andMers199473211
23andMe allrs199473211
SNP Nexus

SNPshotrs199473211
SNPdbers199473211
MSV3drs199473211
GWAS Ctlgrs199473211
Max Magnitude0
ClinVar
Risk rs199473211(C;C)
Alt rs199473211(C;C)
Reference rs199473211(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38608022C>G
CLNSRC ClinVar
CLNACC RCV000058593.2,