"GeneDx"[submitter] AND "LOC129931026"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146007	GRCh38/hg38 1p21.3-13.3(chr1:97272349-108893138)x1	AGL, AKNAD1 +195 more	Copy number loss	See cases	GPathogenic
Select item 60005	GRCh38/hg38 1p21.3-13.3(chr1:97410602-110670510)x1	AGL, AHCYL1 +333 more	Copy number loss	See cases	GPathogenic
Select item 1202872	NM_003672.4(CDC14A):c.49+135A>G	CDC14A, LOC129931026	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1278440	NM_003672.4(CDC14A):c.49+169T>G	CDC14A, LOC129931026	Single nucleotide variant (intron variant)	not provided	GBenign

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