Gene

KCNH2

HGNC: HGNC:6251 | GeneCards: KCNH2
Saudi human-genetics coreAll Saudi-affiliated records

Overview

Approved name
Cytogenetic location
-
Locus type
-
In SaudiVarKB
10 articles, 10 mentions

Synonyms

None recorded

External resources

ClinVar ↗PubMed ↗
10Publications5Co-reported phenotypes
0Reported variants
0ClinVar pathogenic / likely pathogenic
0Saudi regions
OpenLiterature network

Co-reported phenotypes

Phenotypes named in the same articles as KCNH2. Co-mention, not a proven association.

PhenotypeArticlesEvidence
long QT syndrome6View sentences
arrhythmia3View sentences
Down syndrome1View sentences
congenital heart disease1View sentences
hearing loss1View sentences

Reported variants

Variants linked to KCNH2 through dbSNP or LitVar2. ClinVar status is shown for core-subset variants.

No variants with a confirmed gene link.

Saudi regions

Regions or cities named in the abstracts of articles that mention KCNH2.

No Saudi region named.