List of variants in gene AP5Z1 reported as likely pathogenic by Invitae

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: 10

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HGVS	dbSNP	gnomAD frequency
NC_000007.13:g.(?_4816199)_4825153del
NM_014855.3(AP5Z1):c.1132+1_1132+3del	rs2115114032
NM_014855.3(AP5Z1):c.1509_1595+26del
NM_014855.3(AP5Z1):c.1707+1G>A
NM_014855.3(AP5Z1):c.1806-1G>C
NM_014855.3(AP5Z1):c.41+812_970del
NM_014855.3(AP5Z1):c.931+1G>A	rs1583232513
NM_014855.3(AP5Z1):c.970-1G>A
NM_014855.3(AP5Z1):c.970-2A>G
NM_014855.3(AP5Z1):c.970-2_983del	rs1562408256

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