ClinVar Miner

List of variants in gene PKD1 reported as uncertain significance by Genetics and Molecular Pathology, SA Pathology

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001009944.3(PKD1):c.11116A>G (p.Lys3706Glu)	rs2151704349
NM_001009944.3(PKD1):c.12458T>G (p.Val4153Gly)	rs2151678778

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