"GeneDx"[submitter] AND "LOC132089009"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58033	GRCh38/hg38 4q22.3-28.3(chr4:96092893-136410207)x3	LOC129993082, LOC129993083 +661 more	Copy number gain	See cases	GPathogenic
Select item 1233690	NM_018699.4(PRDM5):c.1189-240del	LOC132089009, PRDM5	Deletion (intron variant)	not provided	GBenign
Select item 677849	NM_018699.4(PRDM5):c.1189-242A>T	LOC132089009, PRDM5	Single nucleotide variant (intron variant)	not provided	GBenign

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