List of variants reported as pathogenic for Spermatogenic failure 18 by OMIM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_015512.5(DNAH1):c.3877G>A (p.Asp1293Asn)	rs140883175	0.00034
NM_015512.5(DNAH1):c.11726_11727del (p.Pro3909fs)	rs779490893	0.00004
NM_015512.5(DNAH1):c.11788-1G>A	rs1131692234
NM_015512.5(DNAH1):c.3860T>G (p.Val1287Gly)	rs1131692251
NM_015512.5(DNAH1):c.8626-1G>A	rs1131692250

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