"Laan Lab, Human Genetics Research Group, University of Tartu"[submitt - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2690950	NM_001142966.3(GREB1L):c.23A>C (p.Gln8Pro)	GREB1L, LOC101927521 (Q8P)	Single nucleotide variant (missense variant)	Male infertility with azoospermia or oligozoospermia due to single gene mutation	GLikely pathogenic
Select item 2690951	NM_001142966.3(GREB1L):c.311C>T (p.Pro104Leu)	GREB1L, LOC101927521 (P104L)	Single nucleotide variant (missense variant)	Male infertility with azoospermia or oligozoospermia due to single gene mutation	GLikely pathogenic