ClinVar Miner

Submissions for variant NM_018192.4(P3H2):c.1189-18_1189-17del

dbSNP: rs11311050
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001516400 SCV001724673 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001516400 SCV001915366 benign not provided 2019-08-16 criteria provided, single submitter clinical testing

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