ClinVar Miner

Submissions for variant NM_032409.3(PINK1):c.1124-258A>G

gnomAD frequency: 0.02714  dbSNP: rs115740489
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 RCV001559432 SCV001781655 likely benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001559432 SCV005255949 likely benign not provided criteria provided, single submitter not provided

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