ClinVar Miner

Submissions for variant NM_014336.5(AIPL1):c.784+7G>A

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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 RCV003615221 SCV004522546 likely benign Leber congenital amaurosis 4 2024-01-12 criteria provided, single submitter clinical testing

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