ClinVar Miner

Submissions for variant NM_006892.4(DNMT3B):c.1579T>C (p.Cys527Arg)

dbSNP: rs2146029958
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV001568341 SCV001792197 pathogenic Facioscapulohumeral muscular dystrophy 4, digenic 2021-08-20 no assertion criteria provided literature only

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