ClinVar Miner

Submissions for variant NM_000130.4(F5):c.237A>G (p.Gln79=) (rs6028)

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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 RCV000311703 SCV000351158 likely benign Thrombophilia due to activated protein C resistance 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000366465 SCV000351159 likely benign Budd-Chiari syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000271943 SCV000351160 likely benign Venous thrombosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000327005 SCV000351161 likely benign Factor V deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000311703 SCV000351162 likely benign Thrombophilia due to activated protein C resistance 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000243137 SCV000302413 benign not specified criteria provided, single submitter clinical testing

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