GBA

Name
GBA
HGNC ID
HGNC:4177
Cytogenetic Location
1q22
Haploinsufficiency
Associated with Autosomal Recessive Phenotype
Triplosensitivity
No Evidence
External Resources
View external resources
ClinVar Variants
View ClinVar Variants
GeneReviews®
View GeneReviews
Curated by Classification Date Report
Clinicalactionability on Clinical Actionability View report for scoring details 01/10/2018 View report
Curated by Classification Date Report
Clinicalactionability on Clinical Actionability View report for scoring details 01/10/2018 View report
Curated by Classification Date Report
Clinicalactionability on Clinical Actionability View report for scoring details 01/10/2018 View report
Curated by Classification Date Report
Clinicalactionability on Clinical Actionability View report for scoring details 01/10/2018 View report
Curated by Classification Date Report
Clinicalactionability on Clinical Actionability View report for scoring details 01/10/2018 View report