ClinVar Miner

Submissions for variant NM_018192.4(P3H2):c.481-9dup

dbSNP: rs371335199
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 RCV000966896 SCV001114255 benign not provided 2024-01-13 criteria provided, single submitter clinical testing
GeneDx RCV000966896 SCV001830834 likely benign not provided 2020-03-19 criteria provided, single submitter clinical testing

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