Submissions for variant NM_012120.3(CD2AP):c.219A>G (p.Glu73=)

gnomAD frequency: 0.00843  dbSNP: rs7749045

Total submissions: 5

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
PreventionGenetics, part of Exact Sciences	RCV000242331	SCV000311842	benign	not specified		criteria provided, single submitter	clinical testing
Illumina Laboratory Services, Illumina	RCV000310595	SCV000463759	benign	Focal segmental glomerulosclerosis 3, susceptibility to	2018-01-13	criteria provided, single submitter	clinical testing	This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.
Invitae	RCV000973382	SCV001121139	benign	not provided	2023-12-11	criteria provided, single submitter	clinical testing
GeneDx	RCV000973382	SCV002006802	likely benign	not provided	2020-03-11	criteria provided, single submitter	clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children	RCV002294169	SCV002587425	benign	Focal segmental glomerulosclerosis	2018-10-01	criteria provided, single submitter	clinical testing