List of variants in gene DNAH17 reported as pathogenic 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_173628.4(DNAH17):c.1293_1294del (p.Tyr431_Lys432delinsTer)	rs767723684
NM_173628.4(DNAH17):c.5408G>A (p.Cys1803Tyr)	rs2146716548
NM_173628.4(DNAH17):c.5486G>A (p.Cys1829Tyr)	rs1598595659
NM_173628.4(DNAH17):c.5707C>T (p.Arg1903Cys)	rs775503600
NM_173628.4(DNAH17):c.7994_8012del (p.Gly2665fs)	rs1598525781
NM_173628.4(DNAH17):c.[10496C>T;10784T>C]

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