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rs199473107

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473107(A;A)
Make rs199473107(A;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606078
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473107
ebirs199473107
HLIrs199473107
Exacrs199473107
Varsomers199473107
Maprs199473107
PheGenIrs199473107
hapmaprs199473107
1000 genomesrs199473107
hgdprs199473107
ensemblrs199473107
gopubmedrs199473107
geneviewrs199473107
scholarrs199473107
googlers199473107
pharmgkbrs199473107
gwascentralrs199473107
openSNPrs199473107
23andMers199473107
23andMe allrs199473107
SNP Nexus

SNPshotrs199473107
SNPdbers199473107
MSV3drs199473107
GWAS Ctlgrs199473107
Max Magnitude0
ClinVar
Risk rs199473107(A;A)
Alt rs199473107(A;A)
Reference rs199473107(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38647569A>T
CLNSRC ClinVar
CLNACC RCV000058403.2,