"GenomeConnect - Invitae Patient Insights Network"[submitter] AND "PRO - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 965934	NM_006017.3(PROM1):c.2281-2A>G	PROM1	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 965933	NM_006017.3(PROM1):c.1682+3A>G	PROM1	Single nucleotide variant (intron variant)	not provided	GPathogenic
Select item 194072	NM_006017.3(PROM1):c.1345G>A (p.Val449Met)	PROM1 (V449M +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity

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