ClinVar Miner

Submissions for variant NM_000169.3(GLA):c.999+12_999+13insCATCTTAAA

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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 RCV005197732 SCV005831701 likely benign Fabry disease 2024-03-15 criteria provided, single submitter clinical testing

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