Gene

G6PD

HGNC: HGNC:4057 | GeneCards: G6PD

None recorded

0ClinVar pathogenic / likely pathogenic

Co-reported phenotypes

Phenotypes named in the same articles as G6PD. Co-mention, not a proven association.

Phenotype	Articles	Evidence
glucose-6-phosphate dehydrogenase deficiency	78	View sentences
sickle cell disease	12	View sentences
thalassemia	9	View sentences
sickle cell anemia	8	View sentences
malaria	7	View sentences
diabetes mellitus	5	View sentences
COVID-19	3	View sentences
autism spectrum disorder	3	View sentences
asthma	2	View sentences
colorectal cancer	2	View sentences
epilepsy	2	View sentences
hypertension	2	View sentences
neurodevelopmental disorder	2	View sentences
obesity	2	View sentences
pre-eclampsia	2	View sentences
renal failure	2	View sentences
stroke	2	View sentences
Down syndrome	1	View sentences
Klinefelter syndrome	1	View sentences
arrhythmia	1	View sentences
breast cancer	1	View sentences
congenital cataract	1	View sentences
cystic fibrosis	1	View sentences
dyslipidemia	1	View sentences
familial hypercholesterolemia	1	View sentences

and 12 more

Variants linked to G6PD through dbSNP or LitVar2. ClinVar status is shown for core-subset variants.

Variant	rsID	Articles	ClinVar
G202A	-	2	-
A376G	-	1	-

Regions or cities named in the abstracts of articles that mention G6PD.