List of variants in gene PDZD7 reported as pathogenic for autosomal dominant nonsyndromic hearing loss

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001195263.2(PDZD7):c.2211del (p.Gln737fs)	rs1157689930	0.00004
NM_001195263.2(PDZD7):c.166dup (p.Arg56fs)	rs587776894

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