ClinVar Miner

Submissions for variant NM_000273.3(GPR143):c.360+13C>G

gnomAD frequency: 0.08633  dbSNP: rs11095520
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000253665 SCV000303409 benign not specified criteria provided, single submitter clinical testing
Invitae RCV000084926 SCV001731810 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV000084926 SCV001842487 benign not provided 2019-09-21 criteria provided, single submitter clinical testing
Retina International RCV000084926 SCV000117062 not provided not provided no assertion provided not provided

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