ClinVar Miner

Submissions for variant NM_000312.4(PROC):c.199G>A (p.Glu67Lys)

dbSNP: rs1448630830
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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 RCV000761310 SCV000891290 likely pathogenic Thrombophilia due to protein C deficiency, autosomal dominant 2018-12-27 criteria provided, single submitter clinical testing

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