ClinVar Miner

Submissions for variant NM_001939.3(DRP2):c.1320C>T (p.His440=)

dbSNP: rs146293556
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 RCV000938752 SCV001084575 likely benign not provided 2024-11-30 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005056695 SCV005725991 likely benign not specified 2024-11-25 criteria provided, single submitter clinical testing

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