ClinVar Miner

Submissions for variant NM_000350.3(ABCA4):c.769-32T>C

gnomAD frequency: 0.24162  dbSNP: rs526016
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000250551 SCV000303786 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000085868 SCV001950567 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Retina International RCV000085868 SCV000118011 not provided not provided no assertion provided not provided

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