ClinVar Miner

Submissions for variant NM_020944.3(GBA2):c.-162G>A

dbSNP: rs2132025854
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001848439 SCV002104705 uncertain significance Hereditary spastic paraplegia 2016-12-30 criteria provided, single submitter clinical testing

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