ClinVar for OMIM (Select 604913) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1802187	NM_001367975.1(BTG4):c.285G>C (p.Trp95Cys)	BTG4	Single nucleotide variant (missense variant)	Oocyte maturation defect 8	GPathogenic
Select item 977514	NM_001367975.1(BTG4):c.166G>A (p.Ala56Thr)	BTG4 (A56T)	Single nucleotide variant (missense variant)	Oocyte maturation defect 8	GLikely pathogenic