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rs199473606

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473606(G;T)
Make rs199473606(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38560357
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473606
ebirs199473606
HLIrs199473606
Exacrs199473606
Varsomers199473606
Maprs199473606
PheGenIrs199473606
hapmaprs199473606
1000 genomesrs199473606
hgdprs199473606
ensemblrs199473606
gopubmedrs199473606
geneviewrs199473606
scholarrs199473606
googlers199473606
pharmgkbrs199473606
gwascentralrs199473606
openSNPrs199473606
23andMers199473606
23andMe allrs199473606
SNP Nexus

SNPshotrs199473606
SNPdbers199473606
MSV3drs199473606
GWAS Ctlgrs199473606
Max Magnitude0
ClinVar
Risk rs199473606(A,T;A,T)
Alt rs199473606(A,T;A,T)
Reference rs199473606(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.38601848C>A; NC_000003.11:g.38601848C>T
CLNSRC ClinVar
CLNACC RCV000058631.2, RCV000183059.1,