ClinVar Miner

List of variants in gene combination DPY19L2, LOC130008194 reported as pathogenic 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: 1

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HGVS	dbSNP	gnomAD frequency
NC_000012.12:g.(?_63558913)_(63669201_?)del

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