Variants in gene PKD2 with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000297.4(PKD2):c.1258A>G (p.Arg420Gly)	rs1727651995
NM_000297.4(PKD2):c.1349G>A (p.Gly450Asp)	rs1578135842
NM_000297.4(PKD2):c.2019+5G>A	rs1578142944
NM_000297.4(PKD2):c.2020-5A>G	rs2110133917
NM_000297.4(PKD2):c.2208_2213del (p.Leu736_Asn737del)	rs778896252
NM_000297.4(PKD2):c.2600T>C (p.Leu867Pro)	rs1578153598
NM_000297.4(PKD2):c.773T>C (p.Leu258Pro)	rs2110104859

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