ClinVar Miner

Submissions for variant NM_000130.4(F5):c.4095C>T (p.Thr1365=) (rs9332607)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000360723 SCV000350862 likely benign Thrombophilia due to activated protein C resistance 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000298910 SCV000350863 likely benign Factor V deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000360723 SCV000350864 likely benign Thrombophilia due to activated protein C resistance 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000268268 SCV000350865 likely benign Venous thrombosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000302299 SCV000350866 likely benign Budd-Chiari syndrome 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000243401 SCV000302425 benign not specified criteria provided, single submitter clinical testing

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