Variants in gene PKD1 with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 15

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HGVS	dbSNP	gnomAD frequency
NM_001009944.3(PKD1):c.971G>T (p.Arg324Leu)	rs199476099	0.00351
NM_001009944.3(PKD1):c.9412G>A (p.Val3138Met)	rs1358566538	0.00001
NM_001009944.3(PKD1):c.10958C>T (p.Ala3653Val)	rs1483214870
NM_001009944.3(PKD1):c.11249G>A (p.Arg3750Gln)	rs1327414405
NM_001009944.3(PKD1):c.12448C>T (p.Arg4150Cys)	rs1282668884
NM_001009944.3(PKD1):c.12465T>G (p.Phe4155Leu)	rs2091413514
NM_001009944.3(PKD1):c.1543G>A (p.Gly515Arg)	rs1555458704
NM_001009944.3(PKD1):c.1831C>T (p.Arg611Trp)	rs1555458413
NM_001009944.3(PKD1):c.2180T>C (p.Leu727Pro)	rs1616940
NM_001009944.3(PKD1):c.4825ATC[1] (p.Ile1610del)	rs1567198691
NM_001009944.3(PKD1):c.7300C>T (p.Arg2434Trp)	rs151257298
NM_001009944.3(PKD1):c.8284_8295dup (p.Ile2762_Arg2765dup)	rs1596527370
NM_001009944.3(PKD1):c.8447T>C (p.Leu2816Pro)	rs1567177684
NM_001009944.3(PKD1):c.9404C>T (p.Thr3135Met)	rs1555449635
NM_001009944.3(PKD1):c.974A>G (p.Tyr325Cys)	rs1232180956

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