List of variants in gene CD2AP reported as likely pathogenic for familial nephrotic syndrome

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_012120.3(CD2AP):c.764dup (p.Ser256fs)	rs776297606	0.00001
NM_012120.3(CD2AP):c.1108+1G>T
NM_012120.3(CD2AP):c.1569AGA[2] (p.Glu525del)	rs545551160
NM_012120.3(CD2AP):c.30T>G (p.Tyr10Ter)

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