ClinVar Miner

Submissions for variant NM_030777.4(SLC2A10):c.209A>G (p.Asp70Gly)

dbSNP: rs1979817884
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001058944 SCV001223545 uncertain significance Arterial tortuosity syndrome 2021-08-30 criteria provided, single submitter clinical testing

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