List of variants in gene PKD1 reported as likely benign by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001009944.3(PKD1):c.8293C>T (p.Arg2765Cys)	rs144979397	0.00495
NM_001009944.3(PKD1):c.8344G>A (p.Val2782Met)	rs151089809	0.00053
NM_001009944.3(PKD1):c.7937T>C (p.Ile2646Thr)	rs374500158	0.00029
NM_001009944.3(PKD1):c.9548G>A (p.Arg3183Gln)	rs79648977	0.00020
NM_001009944.3(PKD1):c.8267C>T (p.Thr2756Ile)	rs141296093	0.00013
NM_001009944.3(PKD1):c.2239G>A (p.Ala747Thr)	rs796086075	0.00001

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