ClinVar Miner

Submissions for variant NM_019616.4(F7):c.*846CTTCA[1]

dbSNP: rs886049998
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000314976 SCV000382768 uncertain significance Factor VII deficiency 2016-06-14 criteria provided, single submitter clinical testing

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