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rs199473363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473363(A;A)
Make rs199473363(A;T)
ReferenceGRCh38 38.1/142
Chromosome21
Position34370537
GeneKCNE2
is asnp
is mentioned by
dbSNPrs199473363
ebirs199473363
HLIrs199473363
Exacrs199473363
Varsomers199473363
Maprs199473363
PheGenIrs199473363
hapmaprs199473363
1000 genomesrs199473363
hgdprs199473363
ensemblrs199473363
gopubmedrs199473363
geneviewrs199473363
scholarrs199473363
googlers199473363
pharmgkbrs199473363
gwascentralrs199473363
openSNPrs199473363
23andMers199473363
23andMe allrs199473363
SNP Nexus

SNPshotrs199473363
SNPdbers199473363
MSV3drs199473363
GWAS Ctlgrs199473363
Max Magnitude0
ClinVar
Risk rs199473363(A;A)
Alt rs199473363(A;A)
Reference rs199473363(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNE2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000021.8:g.35742836T>A
CLNSRC ClinVar
CLNACC RCV000058376.2,