ClinVar Miner

Submissions for variant NM_004606.5(TAF1):c.1979G>A (p.Gly660Asp)

dbSNP: rs1602489684
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Medicine, Institute for Basic Research in Developmental Disabilities RCV001027747 SCV000998764 likely pathogenic Intellectual disability, X-linked, syndromic 33 2019-09-23 no assertion criteria provided clinical testing
Yale Center for Mendelian Genomics, Yale University RCV001849455 SCV002106726 association Heart, malformation of 2020-06-13 no assertion criteria provided literature only

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