ClinVar Miner

Submissions for variant NM_017752.3(TBC1D8B):c.20A>G (p.Glu7Gly)

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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 RCV003992083 SCV004811971 uncertain significance Nephrotic syndrome, type 20 2021-09-24 criteria provided, single submitter clinical testing ACMG Criteria: PM2_SUP, PP3 (ACMG Version 3)

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