List of variants reported as pathogenic for spermatogenic failure 33 by OMIM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_144668.6(CFAP251):c.331G>T (p.Glu111Ter)	rs199671406	0.00098
NM_144668.6(CFAP251):c.123del (p.Asp42fs)	rs749163856
NM_144668.6(CFAP251):c.1588_1589del (p.Leu530fs)	rs1565912409
NM_144668.6(CFAP251):c.3007-4915_3338-930del

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