Related gene-specific medical variations for Gene (Select 8556) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3248021	NC_000001.10:g.(?_100963621)_(100964935_?)del	CDC14A	Deletion	not provided	GUncertain significance
Select item 3062711	GRCh37/hg19 1p21.2(chr1:100978713-100997065)x1	CDC14A	Copy number loss	not specified	GUncertain significance
Select item 1278440	NM_003672.4(CDC14A):c.49+169T>G	CDC14A, LOC129931026	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1202872	NM_003672.4(CDC14A):c.49+135A>G	CDC14A, LOC129931026	Single nucleotide variant (intron variant)	not provided	GLikely benign

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