ClinVar Miner

Submissions for variant NM_000128.4(F11):c.-1-138A>C

dbSNP: rs3822057
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001543709 SCV001762527 benign Hereditary factor XI deficiency disease 2021-07-10 criteria provided, single submitter clinical testing
GeneDx RCV001673163 SCV001888048 benign not provided 2018-11-10 criteria provided, single submitter clinical testing

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