ClinVar Miner

Submissions for variant NM_152415.3(VPS37A):c.918G>A (p.Gln306=)

gnomAD frequency: 0.00016  dbSNP: rs370931373
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 RCV003653410 SCV001010890 likely benign Hereditary spastic paraplegia 53 2023-11-09 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003479232 SCV004223139 likely benign not specified 2023-11-22 criteria provided, single submitter clinical testing

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