ClinVar Miner

Submissions for variant NM_021926.4(ALX4):c.2T>C (p.Met1Thr)

dbSNP: rs1475499990
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics Institute, Tel Aviv Sourasky Medical Center RCV001391288 SCV001593237 uncertain significance Optic nerve glioma 2021-05-12 criteria provided, single submitter clinical testing

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