ClinVar Miner

Submissions for variant NM_030777.4(SLC2A10):c.4+10G>A

dbSNP: rs1978796306
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001502809 SCV001707646 likely benign Arterial tortuosity syndrome 2023-09-09 criteria provided, single submitter clinical testing

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