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Items: 4

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
KCNH2Long QT syndrome 1/2, digenicPathogenic
(Mar 23, 1999)
no assertion criteria provided
2.
GRCh37:
Chr7:150646083
GRCh38:
Chr7:150948995
KCNH2Long QT syndrome 2, Congenital long QT syndromePathogenic
(Sep 15, 2000)
no assertion criteria provided
3.
GRCh37:
Chr7:150646072
GRCh38:
Chr7:150948984
KCNH2Long QT syndrome 2, Congenital long QT syndrome, Cardiovascular phenotype
Pathogenic
(Dec 22, 2015)
criteria provided, single submitter
4.
GRCh37:
Chr11:2604765
GRCh38:
Chr11:2583535
KCNQ1Long QT syndrome 1, Long QT syndrome 1/2, digenic, Long QT syndrome,
not provided, Congenital long QT syndrome
Pathogenic
(Aug 6, 2016)
criteria provided, multiple submitters, no conflicts
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