ClinVar Miner

Submissions for variant NM_145167.3(PIGM):c.867C>G (p.Ser289=)

dbSNP: rs776974327
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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 RCV001455796 SCV001659562 likely benign Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency 2022-08-16 criteria provided, single submitter clinical testing

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