List of variants in gene combination LOC124625920, PDE3A reported as benign

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000921.5(PDE3A):c.318A>G (p.Gly106=)	rs77246609	0.00903
NM_000921.5(PDE3A):c.296A>C (p.Glu99Ala)	rs201132768	0.00464
NM_000921.5(PDE3A):c.578T>C (p.Val193Ala)	rs141457914	0.00310
NM_000921.5(PDE3A):c.402G>T (p.Ala134=)	rs145887541	0.00199
NM_000921.5(PDE3A):c.507G>C (p.Gly169=)	rs144296189

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