List of variants in gene PDE3A reported as uncertain significance for bone disorder

Minimum submission review status:		Collection method:
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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
NM_000921.5(PDE3A):c.1289C>T (p.Pro430Leu)	rs375216649	0.00017
NM_000921.5(PDE3A):c.1943A>T (p.Glu648Val)	rs371999647	0.00002
NM_000921.5(PDE3A):c.1903G>C (p.Asp635His)	rs1177411012	0.00001
NM_000921.5(PDE3A):c.1306C>T (p.Arg436Ter)
NM_000921.5(PDE3A):c.1564C>T (p.Leu522Phe)
NM_000921.5(PDE3A):c.2593T>G (p.Leu865Val)	rs1592145544
NM_000921.5(PDE3A):c.2863G>C (p.Ala955Pro)
NM_000921.5(PDE3A):c.3329C>T (p.Ser1110Leu)
NM_000921.5(PDE3A):c.41C>A (p.Pro14His)
NM_000921.5(PDE3A):c.94C>A (p.Arg32Ser)

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