ClinVar Miner

Submissions for variant NM_025137.4(SPG11):c.1603-5T>C

dbSNP: rs2084149728
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001092498 SCV001249037 uncertain significance not provided 2019-11-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003600398 SCV004525254 likely benign Hereditary spastic paraplegia 11 2023-10-13 criteria provided, single submitter clinical testing

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