"GeneDx"[submitter] AND "LOC130008357"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1232496	NM_172240.3(POC1B):c.15+90G>A	LOC130008357, POC1B +2 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1198938	NM_172240.3(POC1B):c.15+27dup	LOC130008357, POC1B +2 more	Duplication (intron variant)	not provided	GLikely benign
Select item 1272979	NM_172240.3(POC1B):c.15+26_15+27del	POC1B-GALNT4, LOC130008357 +2 more	Deletion (intron variant)	not provided	GBenign

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