ClinVar Miner

Submissions for variant NM_000362.5(TIMP3):c.128G>A (p.Arg43Gln)

dbSNP: rs1569273746
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV001073275 SCV001238811 uncertain significance Retinal dystrophy 2018-10-12 criteria provided, single submitter clinical testing

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