ClinVar Miner

Submissions for variant NM_019616.4(F7):c.*888G>A

gnomAD frequency: 0.02191  dbSNP: rs79733913
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000367187 SCV000382769 likely benign Factor VII deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000262422 SCV000483432 likely benign Factor X deficiency 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705274 SCV005218366 likely benign not provided criteria provided, single submitter not provided

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