ClinVar Miner

Submissions for variant NM_001182.5(ALDH7A1):c.1009-6G>A

gnomAD frequency: 0.00500  dbSNP: rs138056453
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000123620 SCV000166959 benign not specified 2012-05-14 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV000472930 SCV000561546 benign Pyridoxine-dependent epilepsy 2024-01-29 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000472930 SCV001316585 likely benign Pyridoxine-dependent epilepsy 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 likely benign is not then subjected to further curation. The score for this variant resulted in a classification of likely benign for this disease.
Genome-Nilou Lab RCV000472930 SCV004048935 benign Pyridoxine-dependent epilepsy 2023-04-11 criteria provided, single submitter clinical testing

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