Submissions for variant NM_000789.4(ACE):c.3692-6G>A

gnomAD frequency: 0.50850  dbSNP: rs4363

Total submissions: 5

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
PreventionGenetics, part of Exact Sciences	RCV000253064	SCV000305527	benign	not specified		criteria provided, single submitter	clinical testing
Illumina Laboratory Services, Illumina	RCV000358043	SCV000404702	benign	Renal tubular dysgenesis	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.
Genome-Nilou Lab	RCV000358043	SCV001768806	benign	Renal tubular dysgenesis	2021-07-14	criteria provided, single submitter	clinical testing
GeneDx	RCV001689803	SCV001910930	benign	not provided	2018-11-10	criteria provided, single submitter	clinical testing
Invitae	RCV001689803	SCV002375743	benign	not provided	2024-01-31	criteria provided, single submitter	clinical testing