"GeneDx"[submitter] AND "GCOM1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57881	GRCh38/hg38 15q21.2-22.2(chr15:50864913-59646577)x1	ADAM10, ALDH1A2 +287 more	Copy number loss	See cases	GPathogenic
Select item 57882	GRCh38/hg38 15q21.3-22.2(chr15:57567950-63019415)x1	ADAM10, ALDH1A2 +163 more	Copy number loss	See cases	GPathogenic
Select item 1275460	NM_015532.5(POLR2M):c.113+151G>C	GCOM1, POLR2M	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1231145	NM_015532.5(POLR2M):c.113+322C>G	GCOM1, POLR2M	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233236	NM_015532.5(POLR2M):c.183C>T (p.Ala61=)	GCOM1, POLR2M	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 1183428	NM_015532.5(POLR2M):c.963+37G>A	GCOM1, POLR2M	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar