ClinVar Miner

Submissions for variant NM_000169.3(GLA):c.972G>A (p.Leu324=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004016117 SCV004824310 likely benign Fabry disease 2023-06-08 criteria provided, single submitter clinical testing

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