List of variants reported as uncertain significance for Spermatogenic failure 39

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_173628.4(DNAH17):c.3650G>C (p.Arg1217Thr)	rs146570590	0.00041
NM_173628.4(DNAH17):c.6389C>T (p.Ala2130Val)	rs771207848	0.00001
NM_173628.4(DNAH17):c.11092G>A (p.Glu3698Lys)
NM_173628.4(DNAH17):c.11204C>T (p.Thr3735Met)
NM_173628.4(DNAH17):c.3041C>T (p.Ala1014Val)	rs186768969
NM_173628.4(DNAH17):c.5114C>T (p.Thr1705Met)
NM_173628.4(DNAH17):c.7144G>C (p.Glu2382Gln)	rs535161506
NM_173628.4(DNAH17):c.7727C>A (p.Ser2576Tyr)

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