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rs199473209

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473209(A;G)
Make rs199473209(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38566542
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473209
ebirs199473209
HLIrs199473209
Exacrs199473209
Varsomers199473209
Maprs199473209
PheGenIrs199473209
hapmaprs199473209
1000 genomesrs199473209
hgdprs199473209
ensemblrs199473209
gopubmedrs199473209
geneviewrs199473209
scholarrs199473209
googlers199473209
pharmgkbrs199473209
gwascentralrs199473209
openSNPrs199473209
23andMers199473209
23andMe allrs199473209
SNP Nexus

SNPshotrs199473209
SNPdbers199473209
MSV3drs199473209
GWAS Ctlgrs199473209
Max Magnitude0
ClinVar
Risk rs199473209(G;G)
Alt rs199473209(G;G)
Reference rs199473209(A;A)
Significance Probable-Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38608033T>C
CLNSRC ClinVar
CLNACC RCV000058590.2,