ClinVar Miner

Submissions for variant NM_001385682.1(MAP4):c.1370A>G (p.Asn457Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Undiagnosed Diseases Network, NIH RCV002509906 SCV002818565 uncertain significance Kleine-Levin syndrome 2017-10-19 no assertion criteria provided clinical testing

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