ClinVar Miner

List of variants in gene PKD1 reported as likely pathogenic by Institute of Human Genetics, University of Wuerzburg

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.10619-1G>A	rs1567159074
NM_001009944.3(PKD1):c.7904dup (p.Arg2636fs)	rs1596536873

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