ClinVar Miner

Submissions for variant NM_001172509.2(SATB2):c.1784del (p.Pro595fs)

dbSNP: rs1692194381
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001090651 SCV001246323 pathogenic not provided 2017-12-01 criteria provided, single submitter clinical testing

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