ClinVar Miner

Submissions for variant NM_004183.4(BEST1):c.907G>T (p.Asp303Tyr)

dbSNP: rs1941816094
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Medical Molecular Genetics, University of Zurich RCV001352947 SCV001548015 likely pathogenic Vitelliform macular dystrophy 2 2021-01-30 criteria provided, single submitter clinical testing

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