ClinVar Miner

Submissions for variant NM_001491.3(GCNT2):c.687T>C (p.Tyr229=)

gnomAD frequency: 0.00670  dbSNP: rs35318346
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000312665 SCV000459248 benign Blood group, I system 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.
Labcorp Genetics (formerly Invitae), Labcorp RCV000559672 SCV000653789 benign Cataract 13 with adult I phenotype 2023-08-10 criteria provided, single submitter clinical testing
GeneDx RCV001753828 SCV001986189 benign not provided 2021-07-27 criteria provided, single submitter clinical testing

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