List of variants reported as benign for Spermatogenic failure 4

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001177949.2(SYCP3):c.-122T>A	rs17031944	0.02365
NM_001177949.2(SYCP3):c.*205G>A	rs17723833	0.01977
NM_001177949.2(SYCP3):c.435A>G (p.Glu145=)	rs78591432	0.01236
NM_001177949.2(SYCP3):c.*183A>G	rs115013475	0.01218
NM_001177949.2(SYCP3):c.-53C>G	rs137993065	0.00166
NM_001177949.2(SYCP3):c.-106A>G	rs143456701	0.00101
NM_001177949.2(SYCP3):c.666A>G (p.Gln222=)	rs190337934	0.00060
NM_001177949.2(SYCP3):c.59A>G (p.Gln20Arg)	rs143228358	0.00020

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