ClinVar Miner

Submissions for variant NM_001110792.2(MECP2):c.1356dup (p.Ala453fs)

dbSNP: rs267608624
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
RettBASE RCV000132987 SCV000187971 pathogenic Rett syndrome 2008-02-18 no assertion criteria provided curation

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