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rs199473206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473206(A;A)
Make rs199473206(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38566554
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473206
ebirs199473206
HLIrs199473206
Exacrs199473206
Varsomers199473206
Maprs199473206
PheGenIrs199473206
hapmaprs199473206
1000 genomesrs199473206
hgdprs199473206
ensemblrs199473206
gopubmedrs199473206
geneviewrs199473206
scholarrs199473206
googlers199473206
pharmgkbrs199473206
gwascentralrs199473206
openSNPrs199473206
23andMers199473206
23andMe allrs199473206
SNP Nexus

SNPshotrs199473206
SNPdbers199473206
MSV3drs199473206
GWAS Ctlgrs199473206
Max Magnitude0
ClinVar
Risk rs199473206(A;A)
Alt rs199473206(A;A)
Reference rs199473206(G;G)
Significance Pathogenic
Disease Brugada syndrome not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38608045C>T
CLNSRC ClinVar
CLNACC RCV000058589.2, RCV000183043.2,