ClinVar Miner

Submissions for variant NM_000340.2(SLC2A2):c.267T>A (p.Ala89=)

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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 RCV002805728 SCV003033337 likely benign Fanconi-Bickel syndrome 2022-10-18 criteria provided, single submitter clinical testing

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