ClinVar Miner

Submissions for variant NM_001351169.2(NT5C2):c.1273-7_1273-4dup

dbSNP: rs747195167
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 RCV002164723 SCV002338603 likely benign Hereditary spastic paraplegia 45 2023-06-15 criteria provided, single submitter clinical testing

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