List of variants in gene combination LOC124625920, PDE3A reported as uncertain significance by Labcorp Genetics (formerly Invitae), Labcorp

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000921.5(PDE3A):c.340G>A (p.Gly114Arg)	rs776509114	0.00005
NM_000921.5(PDE3A):c.293C>A (p.Ala98Glu)	rs200052001
NM_000921.5(PDE3A):c.293C>G (p.Ala98Gly)	rs200052001
NM_000921.5(PDE3A):c.295G>A (p.Glu99Lys)
NM_000921.5(PDE3A):c.419T>A (p.Leu140Gln)	rs1943425581
NM_000921.5(PDE3A):c.506G>C (p.Gly169Ala)	rs760787571
NM_000921.5(PDE3A):c.511dup (p.Glu171fs)	rs780389664
NM_000921.5(PDE3A):c.577G>C (p.Val193Leu)	rs760427474

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