List of variants reported as likely pathogenic for reproductive system disorder by Clinical Bioinformatic Lab, Royan Institute

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005220.3(DLX3):c.263A>G (p.Tyr88Cys)	rs772972332	0.00001
NM_001271862.2(PNLDC1):c.743G>A (p.Gly248Asp)	rs1781557432
NM_001282717.2(STAG3):c.1953_1955del (p.Leu652del)	rs2117315457

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