ClinVar Miner

Submissions for variant NM_014336.5(AIPL1):c.276+16G>A

dbSNP: rs1165122917
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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 RCV002103740 SCV002399689 likely benign Leber congenital amaurosis 4 2021-04-28 criteria provided, single submitter clinical testing

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