ClinVar Miner

Submissions for variant NM_000052.7(ATP7A):c.2145G>A (p.Leu715=)

dbSNP: rs2149095287
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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 RCV002152406 SCV002412012 likely benign Menkes kinky-hair syndrome; Cutis laxa, X-linked; X-linked distal spinal muscular atrophy type 3 2021-08-12 criteria provided, single submitter clinical testing

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