List of variants in gene PDE4D reported as likely benign by Illumina Laboratory Services, Illumina

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001104631.2(PDE4D):c.*4675G>A	rs536451907	0.00050
NM_001104631.1(PDE4D):c.-126A>G	rs543720951	0.00036
NM_001104631.2(PDE4D):c.1197A>G (p.Glu399=)	rs369906474	0.00005
NM_001104631.2(PDE4D):c.1252C>T (p.Arg418Trp)	rs750666346	0.00002
NM_001104631.2(PDE4D):c.1831-7A>G	rs766871489	0.00002
NM_001104631.2(PDE4D):c.*1200T>A	rs577495801
NM_001104631.2(PDE4D):c.*1201A>T	rs559220819
NM_001104631.2(PDE4D):c.1634_1635dup	rs138187044
NM_001104631.2(PDE4D):c.2242_2243del	rs148755437
NM_001104631.2(PDE4D):c.496_500dup	rs527630861
NM_001104631.2(PDE4D):c.*793GTTT[3]	rs200995197
NM_001104631.2(PDE4D):c.1288-8dup	rs143090133
NM_001104631.2(PDE4D):c.758+11C>A	rs202215336

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