List of variants in gene CC2D2A reported as pathogenic for familial cystic renal disease

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001378615.1(CC2D2A):c.1149+1G>A	rs1553827236
NM_001378615.1(CC2D2A):c.1751G>A (p.Trp584Ter)	rs980305935
NM_001378615.1(CC2D2A):c.3293T>G (p.Leu1098Ter)	rs1719950579
NM_001378615.1(CC2D2A):c.4179+1del	rs386833760

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