ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2222+73A>G

gnomAD frequency: 0.06356  dbSNP: rs1800341
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001540677 SCV001758583 benign not provided 2019-02-11 criteria provided, single submitter clinical testing
Natera, Inc. RCV001836443 SCV002092623 likely benign Fanconi anemia 2017-05-16 no assertion criteria provided clinical testing

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