ClinVar Miner

Submissions for variant NM_000169.3(GLA):c.639+7T>C

gnomAD frequency: 0.00001  dbSNP: rs1555985507
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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 RCV002106377 SCV002439754 likely benign Fabry disease 2021-06-21 criteria provided, single submitter clinical testing

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