ClinVar Miner

Submissions for variant NM_030777.4(SLC2A10):c.54T>A (p.Gly18=)

dbSNP: rs772186491
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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 RCV003009353 SCV003299182 likely benign Arterial tortuosity syndrome 2023-07-17 criteria provided, single submitter clinical testing

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