List of variants reported as uncertain significance for spermatogenic failure 56

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001372106.1(DNAH10):c.7955C>T (p.Thr2652Met)	rs764317091	0.00008
NM_001372106.1(DNAH10):c.6017G>A (p.Arg2006Gln)	rs369904884	0.00005
NM_001372106.1(DNAH10):c.12241C>T (p.Arg4081Cys)	rs755346965	0.00001
NM_001372106.1(DNAH10):c.11893_11896del (p.Asp3965fs)
NM_001372106.1(DNAH10):c.4942T>C (p.Cys1648Arg)
NM_001372106.1(DNAH10):c.7331C>T (p.Ala2444Val)

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