ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.*412G>A (rs972128957)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Aziz Sancar Institute of Experimental Medicine,Istanbul University RCV000736007 SCV000611860 likely pathogenic Somatotroph adenoma 2017-12-05 criteria provided, single submitter research A novel variant associated with clinical findings.

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