"Johns Hopkins Genomics, Johns Hopkins University"[submitter] AND "ZNF - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 977102	NM_020832.3(ZNF687):c.1695C>G (p.His565Gln)	ZNF687 (H565Q)	Single nucleotide variant (missense variant)	Paget disease of bone 6 +1 more	GUncertain significance
Select item 801543	NM_020832.3(ZNF687):c.2810C>A (p.Pro937His)	ZNF687 (P937H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance