ClinVar Miner

Submissions for variant NM_000789.4(ACE):c.1215C>T (p.Pro405=)

gnomAD frequency: 0.35804  dbSNP: rs4309
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000247405 SCV000305520 benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000287918 SCV000404652 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 RCV000287918 SCV001768799 benign Renal tubular dysgenesis 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001651138 SCV001864445 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Invitae RCV001651138 SCV002402316 benign not provided 2024-01-31 criteria provided, single submitter clinical testing

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