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Variant Pathogenicity
CCDC103
Name
CCDC103
HGNC ID
HGNC:32700
Cytogenetic Location
17q21.31
Haploinsufficiency
Associated with Autosomal Recessive Phenotype
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ClinVar Variants
CCDC103
-
primary ciliary dyskinesia 17
| MONDO:0013854
Curated by
Classification
Date
Report
Dosage Sensitivity
Gene Associated with Autosomal Recessive Phenotype
05/31/2017
View report
CCDC103
Curated by
Classification
Date
Report
Dosage Sensitivity
Gene Associated with Autosomal Recessive Phenotype
05/31/2017
View report
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