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rs141423405

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141423405(C;T)
Make rs141423405(T;T)
ReferenceGRCh38 38.1/142
Chromosome21
Position34370707
GeneKCNE2
is asnp
is mentioned by
dbSNPrs141423405
ebirs141423405
HLIrs141423405
Exacrs141423405
Varsomers141423405
Maprs141423405
PheGenIrs141423405
hapmaprs141423405
1000 genomesrs141423405
hgdprs141423405
ensemblrs141423405
gopubmedrs141423405
geneviewrs141423405
scholarrs141423405
googlers141423405
pharmgkbrs141423405
gwascentralrs141423405
openSNPrs141423405
23andMers141423405
23andMe allrs141423405
SNP Nexus

SNPshotrs141423405
SNPdbers141423405
MSV3drs141423405
GWAS Ctlgrs141423405
Max Magnitude0
ClinVar
Risk rs141423405(T;T)
Alt rs141423405(T;T)
Reference rs141423405(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome Long QT syndrome not specified
Variation info
Gene KCNE2
CLNDBN Congenital long QT syndrome Long QT syndrome not specified
Reversed 0
HGVS NC_000021.8:g.35743006C>T
CLNSRC ClinVar University of Washington
CLNACC RCV000058367.2, RCV000148522.1, RCV000170957.3,