ClinVar Miner

Submissions for variant NM_001199097.2(BAIAP3):c.1091G>C (p.Gly364Ala)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003395170 SCV004133686 benign not provided 2022-10-01 criteria provided, single submitter clinical testing BAIAP3: BS1, BS2

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