ClinVar Miner

Submissions for variant NM_000312.4(PROC):c.1166G>C (p.Gly389Ala)

dbSNP: rs1305782685
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota RCV000761311 SCV000891291 likely pathogenic Thrombophilia due to protein C deficiency, autosomal dominant 2018-12-27 criteria provided, single submitter clinical testing

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