List of variants in gene DPY19L2 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_173812.5(DPY19L2):c.869G>A (p.Arg290His)	rs147579680	0.00023
NM_173812.5(DPY19L2):c.1183del (p.Ser395fs)	rs751879424	0.00003
NM_173812.5(DPY19L2):c.1218+1G>A	rs868256749	0.00003
NM_173812.5(DPY19L2):c.2038A>T (p.Lys680Ter)	rs587777205	0.00003
NM_173812.5(DPY19L2):c.893G>A (p.Arg298His)	rs752764341	0.00002
NM_173812.5(DPY19L2):c.892C>T (p.Arg298Cys)	rs587777206	0.00001
NG_031909.1:g.(12232_26209)_(29173_47048)del

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