List of variants in gene combination CD2AP, CD2AP-DT, LOC129996604 reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_012120.3(CD2AP):c.-197C>T	rs886061513	0.00039
NM_012120.3(CD2AP):c.-438C>T	rs191920077	0.00016
NM_012120.3(CD2AP):c.-324G>C	rs886061512	0.00001
NM_012120.3(CD2AP):c.-191G>A	rs886061514
NM_012120.3(CD2AP):c.-329C>T	rs886061511

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