ClinVar Miner

Submissions for variant NM_014921.5(ADGRL1):c.2644G>T (p.Gly882Trp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MVZ Medizinische Genetik Mainz RCV003992081 SCV004811969 uncertain significance Developmental delay, behavioral abnormalities, and neuropsychiatric disorders 2022-11-18 criteria provided, single submitter clinical testing ACMG Criteria: PM2_SUP,PP2,PP3

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