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rs199473569

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473569(A;A)
Make rs199473569(A;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606051
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473569
ebirs199473569
HLIrs199473569
Exacrs199473569
Varsomers199473569
Maprs199473569
PheGenIrs199473569
hapmaprs199473569
1000 genomesrs199473569
hgdprs199473569
ensemblrs199473569
gopubmedrs199473569
geneviewrs199473569
scholarrs199473569
googlers199473569
pharmgkbrs199473569
gwascentralrs199473569
openSNPrs199473569
23andMers199473569
23andMe allrs199473569
SNP Nexus

SNPshotrs199473569
SNPdbers199473569
MSV3drs199473569
GWAS Ctlgrs199473569
Max Magnitude0
ClinVar
Risk rs199473569(A;A)
Alt rs199473569(A;A)
Reference rs199473569(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38647542G>T
CLNSRC ClinVar
CLNACC RCV000058410.2,