ClinVar Miner

Submissions for variant NM_003119.4(SPG7):c.1092G>A (p.Thr364=)

gnomAD frequency: 0.00001  dbSNP: rs771190749
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001473208 SCV001677353 likely benign Hereditary spastic paraplegia 7 2022-08-23 criteria provided, single submitter clinical testing

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