ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.2578+10CCCGCTCCCTGCT[3]

dbSNP: rs3831019
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 RCV000861008 SCV001001206 likely benign Hereditary spastic paraplegia 49 2024-10-29 criteria provided, single submitter clinical testing
Natera, Inc. RCV000861008 SCV002091129 benign Hereditary spastic paraplegia 49 2019-09-25 no assertion criteria provided clinical testing

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