ClinVar Miner

Submissions for variant NM_000052.7(ATP7A):c.2391G>A (p.Leu797=)

dbSNP: rs1603385697
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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 RCV001441810 SCV001644748 likely benign Menkes kinky-hair syndrome; Cutis laxa, X-linked; X-linked distal spinal muscular atrophy type 3 2018-12-10 criteria provided, single submitter clinical testing

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