ClinVar Miner

Submissions for variant NM_001379228.1(MRAP):c.1A>G (p.Met1Val)

dbSNP: rs1555897462
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München RCV000512739 SCV000608361 pathogenic Glucocorticoid deficiency 1 2017-09-30 criteria provided, single submitter clinical testing

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