ClinVar Miner

Submissions for variant NM_000350.3(ABCA4):c.1761-54G>A

gnomAD frequency: 0.23727  dbSNP: rs4147833
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 RCV000085423 SCV001751396 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Retina International RCV000085423 SCV000117560 not provided not provided no assertion provided not provided

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