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rs199473214

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473214(A;G)
Make rs199473214(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38566491
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473214
ebirs199473214
HLIrs199473214
Exacrs199473214
Varsomers199473214
Maprs199473214
PheGenIrs199473214
hapmaprs199473214
1000 genomesrs199473214
hgdprs199473214
ensemblrs199473214
gopubmedrs199473214
geneviewrs199473214
scholarrs199473214
googlers199473214
pharmgkbrs199473214
gwascentralrs199473214
openSNPrs199473214
23andMers199473214
23andMe allrs199473214
SNP Nexus

SNPshotrs199473214
SNPdbers199473214
MSV3drs199473214
GWAS Ctlgrs199473214
Max Magnitude0
ClinVar
Risk rs199473214(G;G)
Alt rs199473214(G;G)
Reference rs199473214(A;A)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38607982T>C
CLNSRC ClinVar
CLNACC RCV000058600.2,