List of variants reported as uncertain significance for Spermatogenic failure 18 by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015512.5(DNAH1):c.10895G>A (p.Arg3632His)	rs562263699	0.00014
NM_015512.5(DNAH1):c.11552G>A (p.Arg3851His)	rs757435709	0.00002
NM_015512.5(DNAH1):c.6065_6066delinsTC (p.Trp2022Phe)
NM_015512.5(DNAH1):c.9395G>A (p.Arg3132His)

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