ClinVar Miner

Submissions for variant NM_019616.4(F7):c.*1240C>G

dbSNP: rs3093256
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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 RCV000286328 SCV000382776 likely benign Factor VII deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000353676 SCV000483434 likely benign Factor X deficiency 2016-06-14 criteria provided, single submitter clinical testing

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