ClinVar Miner

Submissions for variant NM_032638.5(GATA2):c.959G>A (p.Gly320Asp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005031092 SCV005659416 uncertain significance Acute myeloid leukemia; Deafness-lymphedema-leukemia syndrome; Monocytopenia with susceptibility to infections; Myelodysplastic syndrome 2024-04-18 criteria provided, single submitter clinical testing

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