ClinVar Miner

Submissions for variant NM_000350.3(ABCA4):c.2383-13C>T

gnomAD frequency: 0.00026  dbSNP: rs56026711
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001497832 SCV001702569 likely benign not provided 2024-01-24 criteria provided, single submitter clinical testing
GeneDx RCV001497832 SCV001834439 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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