ClinVar Miner

Submissions for variant NM_000312.4(PROC):c.852G>A (p.Glu284=)

gnomAD frequency: 0.00001  dbSNP: rs780286813
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001430246 SCV001632978 likely benign Thrombophilia due to protein C deficiency, autosomal dominant 2021-04-15 criteria provided, single submitter clinical testing

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