ClinVar Miner

Submissions for variant NM_148960.3(CLDN19):c.277G>C (p.Val93Leu)

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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 RCV005015779 SCV005648380 uncertain significance Renal hypomagnesemia 5 with ocular involvement 2024-03-11 criteria provided, single submitter clinical testing

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