ClinVar Miner

Submissions for variant NM_019616.4(F7):c.*533A>C

gnomAD frequency: 0.00744  dbSNP: rs116688254
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000386699 SCV000382755 likely benign Factor VII deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000369304 SCV000483428 likely benign Factor X deficiency 2016-06-14 criteria provided, single submitter clinical testing

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