ClinVar Miner

Submissions for variant NM_022089.4(ATP13A2):c.*24C>T (rs375521810)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV000513473 SCV000608462 uncertain significance not provided 2017-04-30 criteria provided, single submitter clinical testing
GenomeConnect, ClinGen RCV000509196 SCV000607065 not provided Parkinson disease 9 no assertion provided phenotyping only GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.

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