List of variants reported as uncertain significance for Spermatogenic failure 56 by SIB Swiss Institute of Bioinformatics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001372106.1(DNAH10):c.7955C>T (p.Thr2652Met)	rs764317091	0.00007
NM_001372106.1(DNAH10):c.6017G>A (p.Arg2006Gln)	rs369904884	0.00005
NM_001372106.1(DNAH10):c.12241C>T (p.Arg4081Cys)	rs755346965	0.00002

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