ClinVar Miner

Submissions for variant NM_004992.3(MECP2):c.1159_1160delinsT (p.Pro387fs) (rs267608590)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
RettBASE RCV000132904 SCV000187885 pathogenic Rett syndrome 2011-11-01 no assertion criteria provided curation
RettBASE RCV000170101 SCV000222422 pathogenic Mental retardation, X-linked, syndromic 13 2011-11-01 no assertion criteria provided curation

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