ClinVar Miner

Submissions for variant NM_001172509.2(SATB2):c.701-12A>T

dbSNP: rs116585116
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001334831 SCV001527799 uncertain significance Chromosome 2q32-q33 deletion syndrome 2018-04-22 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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