ClinVar Miner

Submissions for variant NM_000444.6(PHEX):c.1303-1G>C (rs1556036014)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Klinikum rechts der Isar RCV000505495 SCV000599633 pathogenic Familial X-linked hypophosphatemic vitamin D refractory rickets 2015-04-14 criteria provided, single submitter clinical testing

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