List of variants in gene SPATA16 reported as likely benign for spermatogenic failure

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_031955.6(SPATA16):c.1577T>C (p.Met526Thr)	rs62622782	0.01931
NM_031955.6(SPATA16):c.1526C>T (p.Ala509Val)	rs115095786	0.01910
NM_031955.6(SPATA16):c.149A>G (p.Asn50Ser)	rs16846624	0.01264
NM_031955.6(SPATA16):c.1143A>G (p.Gln381=)	rs73041295	0.00685
NM_031955.6(SPATA16):c.-121G>A	rs189972919	0.00657
NM_031955.6(SPATA16):c.1365G>T (p.Val455=)	rs199707743	0.00001

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