ClinVar Miner

Submissions for variant NM_030777.4(SLC2A10):c.246C>T (p.Asn82=)

dbSNP: rs2515586814
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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 RCV003504130 SCV004276423 likely benign Arterial tortuosity syndrome 2024-09-27 criteria provided, single submitter clinical testing

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