ClinVar Miner

Submissions for variant NM_001939.3(DRP2):c.1401C>T (p.Asn467=)

gnomAD frequency: 0.00027  dbSNP: rs373791161
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 RCV000936401 SCV001082166 benign not provided 2024-12-13 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005236456 SCV005886602 likely benign not specified 2025-02-04 criteria provided, single submitter clinical testing

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