ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2432G>A (p.Gly811Asp)

dbSNP: rs201152989
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000458018 SCV000547738 benign Fanconi anemia 2024-01-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001274572 SCV002786383 uncertain significance Fanconi anemia complementation group A 2022-05-15 criteria provided, single submitter clinical testing
Natera, Inc. RCV001274572 SCV001458828 uncertain significance Fanconi anemia complementation group A 2019-10-28 no assertion criteria provided clinical testing

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