ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.5901T>C (p.Ser1967=)

gnomAD frequency: 0.00011  dbSNP: rs375558533
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000861437 SCV001001747 likely benign Fanconi anemia 2023-10-18 criteria provided, single submitter clinical testing

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