"ZC4H2-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 707771	NM_018684.4(ZC4H2):c.592C>A (p.Arg198=)	ZC4H2	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 2915631	NM_018684.4(ZC4H2):c.499G>C (p.Val167Leu)	ZC4H2 (V144L +1 more)	Single nucleotide variant (missense variant +2 more)	ZC4H2-related condition +1 more	GBenign/Likely benign
Select item 1785046	NM_018684.4(ZC4H2):c.204G>T (p.Leu68=)	ZC4H2	Single nucleotide variant (synonymous variant +1 more)	ZC4H2-related condition +1 more	GLikely benign

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