ClinVar Miner

Submissions for variant NM_000026.4(ADSL):c.701+113A>G

gnomAD frequency: 0.03257  dbSNP: rs73885691
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 RCV001666768 SCV001884619 benign not provided 2019-08-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001666768 SCV005278819 benign not provided criteria provided, single submitter not provided

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