List of variants reported as likely benign for spermatogenic failure 25

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001350162.2(TEX15):c.2441C>T (p.Pro814Leu)	rs767325029	0.00001
NM_001350162.2(TEX15):c.6127G>A (p.Glu2043Lys)	rs760194002	0.00001
NM_001350162.2(TEX15):c.2672A>T (p.His891Leu)	rs199659098
NM_001350162.2(TEX15):c.4944C>G (p.Asp1648Glu)	rs117362953
NM_001350162.2(TEX15):c.5315G>A (p.Cys1772Tyr)	rs376683373

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