List of variants in gene TTC29 reported as pathogenic for male infertility

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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_031956.4(TTC29):c.330_334del (p.Glu111fs)	rs766352190	0.00004
NM_031956.4(TTC29):c.*334G>A	rs1579486914
NM_031956.4(TTC29):c.1107C>G (p.Tyr369Ter)	rs1489738488
NM_031956.4(TTC29):c.412_425del (p.Asp138fs)	rs1579951018
NM_031956.4(TTC29):c.750C>A (p.Tyr250Ter)	rs763399136
NM_031956.4(TTC29):c.977+1G>T	rs1579787268

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