Variants in gene PKD2 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000297.4(PKD2):c.2398A>C (p.Met800Leu)	rs2234917	0.00481
NM_000297.4(PKD2):c.2411G>A (p.Ser804Asn)	rs145343957	0.00280
NM_000297.4(PKD2):c.1445T>G (p.Phe482Cys)	rs75762896	0.00176
NM_000297.4(PKD2):c.*552G>A	rs139787413	0.00123

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