ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.918G>A (p.Thr306=) (rs199634699)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000248944 SCV000302512 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV000870375 SCV001011869 likely benign Fanconi anemia 2019-12-31 criteria provided, single submitter clinical testing

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