"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 2690976	NM_001347721.2(DYRK1A):c.371G>A (p.Arg124Gln)	DYRK1A (R124Q +2 more)	Single nucleotide variant (missense variant)	Male infertility with spermatogenesis disorder	GLikely pathogenic
Select item 2690977	NM_001347721.2(DYRK1A):c.994G>T (p.Ala332Ser)	DYRK1A (A303S +2 more)	Single nucleotide variant (missense variant)	Male infertility with spermatogenesis disorder	GLikely pathogenic