ClinVar Miner

Submissions for variant NM_005862.3(STAG1):c.42_44dup (p.Asn14_Glu15insAsp)

dbSNP: rs1939944359
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001329476 SCV001520929 uncertain significance Intellectual disability, autosomal dominant 47 2019-06-28 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Labcorp Genetics (formerly Invitae), Labcorp RCV002546325 SCV003021282 likely benign not provided 2024-09-09 criteria provided, single submitter clinical testing

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