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

Submission 1 (other) minimum review status:		Submission 1 (other) 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001009944.3(PKD1):c.5132C>T (p.Thr1711Ile)	rs750076336	0.00003
NM_001009944.3(PKD1):c.127C>G (p.Pro43Ala)	rs1114167365	0.00002

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