List of variants in gene combination MIR1225, PKD1 reported as likely benign for PKD1-related disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001009944.3(PKD1):c.12445-30G>A	rs368570774	0.00003
NM_001009944.3(PKD1):c.12445-18C>T	rs752457130	0.00001
NM_001009944.3(PKD1):c.12445-22T>A

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