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Variant Pathogenicity
CDC14A
Name
CDC14A
HGNC ID
HGNC:1718
Cytogenetic Location
1p21.2
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ClinVar Variants
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ClinVar Variants
CDC14A
-
hearing impairment and infertile male syndrome
| MONDO:0100069
Curated by
Classification
Date
Report
Gene-Disease Validity
Strong
Autosomal Recessive
03/11/2020
View report
CDC14A
-
nonsyndromic genetic deafness
| MONDO:0019497
Curated by
Classification
Date
Report
Gene-Disease Validity
Limited
Autosomal Recessive
02/26/2018
View report
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