ClinVar Miner

Submissions for variant NM_001605.3(AARS1):c.1072-16G>A

gnomAD frequency: 0.00001  dbSNP: rs1323685357
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002972401 SCV003290345 likely benign Charcot-Marie-Tooth disease type 2 2024-06-05 criteria provided, single submitter clinical testing

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