ClinVar Miner

Submissions for variant NM_000169.3(GLA):c.906C>T (p.His302=)

dbSNP: rs1928165990
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001189806 SCV001357170 likely benign Fabry disease 2019-06-26 criteria provided, single submitter clinical testing

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