ClinVar Miner

Submissions for variant NM_000130.4(F5):c.1238T>C (p.Met413Thr) (rs6033)

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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 RCV000316570 SCV000351078 likely benign Budd-Chiari syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000373337 SCV000351079 likely benign Thrombophilia due to activated protein C resistance 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000262383 SCV000351080 likely benign Factor V deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000319863 SCV000351081 likely benign Venous thrombosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000373337 SCV000351082 likely benign Thrombophilia due to activated protein C resistance 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000252189 SCV000302404 benign not specified criteria provided, single submitter clinical testing

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