ClinVar Miner

Submissions for variant NM_032575.3(GLIS2):c.80C>A (p.Thr27Lys)

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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 RCV005009800 SCV005639114 uncertain significance Nephronophthisis 7 2024-02-03 criteria provided, single submitter clinical testing

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