ClinVar Miner

Submissions for variant NM_000312.4(PROC):c.1267G>A (p.Gly423Ser)

dbSNP: rs1688706297
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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 RCV001731126 SCV001981531 likely pathogenic Thrombophilia due to protein C deficiency, autosomal dominant 2021-07-01 criteria provided, single submitter clinical testing

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