ClinVar Miner

Submissions for variant NM_014946.4(SPAST):c.870+122A>G

gnomAD frequency: 0.03345  dbSNP: rs72796859
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
GeneDx RCV001565936 SCV001789384 likely benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001565936 SCV005263352 likely benign not provided criteria provided, single submitter not provided

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