"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZNF687"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2721623	NM_020832.3(ZNF687):c.225A>G (p.Pro75=)	ZNF687	Single nucleotide variant (synonymous variant)	ZNF687-related condition +1 more	GLikely benign
Select item 1611976	NM_020832.3(ZNF687):c.276C>T (p.Pro92=)	ZNF687	Single nucleotide variant (synonymous variant)	ZNF687-related condition +1 more	GBenign
Select item 2075548	NM_020832.3(ZNF687):c.527C>T (p.Pro176Leu)	ZNF687 (P176L)	Single nucleotide variant (missense variant)	ZNF687-related condition +1 more	GLikely benign
Select item 1659135	NM_020832.3(ZNF687):c.776G>A (p.Gly259Glu)	ZNF687 (G259E)	Single nucleotide variant (missense variant)	ZNF687-related condition +1 more	GBenign
Select item 2045492	NM_020832.3(ZNF687):c.1518C>T (p.Asn506=)	ZNF687	Single nucleotide variant (synonymous variant)	ZNF687-related condition +1 more	GBenign/Likely benign
Select item 2049542	NM_020832.3(ZNF687):c.2901G>C (p.Leu967=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2967384	NM_020832.3(ZNF687):c.2964+3G>A	ZNF687	Single nucleotide variant (intron variant)	ZNF687-related condition +1 more	GConflicting classifications of pathogenicity
Select item 3044761	NM_020832.3(ZNF687):c.*10C>G	ZNF687	Single nucleotide variant (3 prime UTR variant)	ZNF687-related condition	GBenign

ClinVar