ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.*232G>A

gnomAD frequency: 0.05342  dbSNP: rs7155480
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
GeneDx RCV001674452 SCV001887662 benign not provided 2019-03-20 criteria provided, single submitter clinical testing

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