List of variants in gene PDE4D reported as likely pathogenic for bone development disease

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
NM_001104631.2(PDE4D):c.2051A>G (p.Glu684Gly)	rs1743358464
NM_001104631.2(PDE4D):c.569C>T (p.Ser190Phe)	rs1751144333
NM_001104631.2(PDE4D):c.665T>C (p.Ile222Thr)

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