ClinVar Miner

Submissions for variant NM_022725.3(FANCF):c.373G>A (p.Asp125Asn) (rs61752920)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000857633 SCV000290670 benign not provided 2019-02-06 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000232655 SCV000370173 uncertain significance Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000857633 SCV001148211 likely benign not provided 2018-11-01 criteria provided, single submitter clinical testing
ITMI RCV000121028 SCV000085196 not provided not specified 2013-09-19 no assertion provided reference population

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