ClinVar Miner

Submissions for variant NM_000128.4(F11):c.1576+51C>A

dbSNP: rs2289254
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001543711 SCV001762531 likely benign Hereditary factor XI deficiency disease 2021-07-10 criteria provided, single submitter clinical testing
GeneDx RCV001685473 SCV001897898 benign not provided 2021-05-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001685473 SCV005256809 likely benign not provided criteria provided, single submitter not provided

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