ClinVar Miner

Submissions for variant NM_001605.3(AARS1):c.962+103G>A

gnomAD frequency: 0.08458  dbSNP: rs7193598
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 RCV001695436 SCV001914000 benign not provided 2018-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001695436 SCV005248061 benign not provided criteria provided, single submitter not provided

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