ClinVar Miner

Submissions for variant NM_000026.4(ADSL):c.792+148A>C

gnomAD frequency: 0.02425  dbSNP: rs17001857
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 RCV001665863 SCV001881319 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001665863 SCV005278820 benign not provided criteria provided, single submitter not provided

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