ClinVar Miner

Submissions for variant NM_001605.3(AARS1):c.828C>G (p.Ala276=)

gnomAD frequency: 0.00002  dbSNP: rs914414911
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV001121948 SCV001280613 uncertain significance Charcot-Marie-Tooth disease axonal type 2N 2017-04-27 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases did not allow this variant to be ruled in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.
Invitae RCV003744731 SCV004523477 likely benign Charcot-Marie-Tooth disease type 2 2024-01-06 criteria provided, single submitter clinical testing

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