ClinVar Miner

List of variants in gene DPY19L2 reported as uncertain significance for male infertility with teratozoospermia due to single gene mutation

Included ClinVar conditions (6):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NC_000012.11:g.63952693_64062354del
NM_173812.5(DPY19L2):c.1616A>G (p.His539Arg)
NM_173812.5(DPY19L2):c.1816C>T (p.Arg606Cys)

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