ClinVar Miner

Submissions for variant NM_000130.4(F5):c.2301A>G (p.Ser767=) (rs6021)

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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 RCV000327776 SCV000350995 likely benign Thrombophilia due to activated protein C resistance 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000327776 SCV000350996 likely benign Thrombophilia due to activated protein C resistance 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000273923 SCV000350997 likely benign Budd-Chiari syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000333614 SCV000350998 likely benign Factor V deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000387652 SCV000350999 likely benign Venous thrombosis 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000249734 SCV000302412 benign not specified criteria provided, single submitter clinical testing

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