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rs199473568

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473568(A;G)
Make rs199473568(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606072
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473568
ebirs199473568
HLIrs199473568
Exacrs199473568
Varsomers199473568
Maprs199473568
PheGenIrs199473568
hapmaprs199473568
1000 genomesrs199473568
hgdprs199473568
ensemblrs199473568
gopubmedrs199473568
geneviewrs199473568
scholarrs199473568
googlers199473568
pharmgkbrs199473568
gwascentralrs199473568
openSNPrs199473568
23andMers199473568
23andMe allrs199473568
SNP Nexus

SNPshotrs199473568
SNPdbers199473568
MSV3drs199473568
GWAS Ctlgrs199473568
Max Magnitude0
ClinVar
Risk rs199473568(G;G)
Alt rs199473568(G;G)
Reference rs199473568(A;A)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38647563T>C
CLNSRC ClinVar
CLNACC RCV000058404.2,