ClinVar Miner

Submissions for variant NM_020638.3(FGF23):c.446T>C (p.Met149Thr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005009040 SCV005635057 uncertain significance Autosomal dominant hypophosphatemic rickets; Tumoral calcinosis, hyperphosphatemic, familial, 2 2024-02-20 criteria provided, single submitter clinical testing

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