ClinVar Miner

Submissions for variant NM_030777.4(SLC2A10):c.1611C>A (p.Ile537=)

dbSNP: rs1060502314
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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 RCV002162942 SCV002417918 likely benign Arterial tortuosity syndrome 2021-10-06 criteria provided, single submitter clinical testing

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