ClinVar Miner

Submissions for variant NM_012431.3(SEMA3E):c.1366+85G>A

gnomAD frequency: 0.05316  dbSNP: rs12532427
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 RCV001696573 SCV001916267 benign not provided 2018-08-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001696573 SCV005269690 benign not provided criteria provided, single submitter not provided

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