ClinVar Miner

Submissions for variant NM_012414.4(RAB3GAP2):c.1126G>A (p.Val376Ile)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002908520 SCV003249544 benign Martsolf syndrome; Warburg micro syndrome 2 2022-05-08 criteria provided, single submitter clinical testing

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