ClinVar Miner

Submissions for variant NM_030777.4(SLC2A10):c.645G>C (p.Arg215=)

dbSNP: rs367742782
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001482494 SCV001686868 likely benign Arterial tortuosity syndrome 2023-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001581156 SCV001812730 likely benign not provided 2019-12-03 criteria provided, single submitter clinical testing

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