ClinVar Miner

Submissions for variant NM_000169.3(GLA):c.801+15C>A

dbSNP: rs1191412478
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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 RCV002087866 SCV002377976 likely benign Fabry disease 2024-02-25 criteria provided, single submitter clinical testing

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