List of variants in gene PDE1C reported as benign for autosomal dominant nonsyndromic hearing loss

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001191057.4(PDE1C):c.1773C>T (p.Asn591=)	rs1860790	0.96972
NM_001191057.4(PDE1C):c.1203+28A>G	rs2270218	0.75344
NM_001322059.2(PDE1C):c.471G>A (p.Glu157=)	rs977626	0.43760
NM_001191057.4(PDE1C):c.1782C>T (p.Ala594=)	rs2302450	0.23084
NM_001191057.4(PDE1C):c.1830T>C (p.Gly610=)	rs3213709	0.19854

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