ClinVar Miner

Submissions for variant NM_000130.4(F5):c.552G>T (p.Ser184=) (rs6022)

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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 RCV000394574 SCV000351128 likely benign Thrombophilia due to activated protein C resistance 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000290429 SCV000351129 likely benign Venous thrombosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000345339 SCV000351130 likely benign Budd-Chiari syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000394574 SCV000351131 likely benign Thrombophilia due to activated protein C resistance 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000305953 SCV000351132 likely benign Factor V deficiency 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000249494 SCV000302429 benign not specified criteria provided, single submitter clinical testing

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