ClinVar Miner

Submissions for variant NM_001379110.1(SLC9A6):c.1195-4_1201delinsAGGTTGCTG

dbSNP: rs2071146308
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
Diagnostic Laboratory, Strasbourg University Hospital RCV001257722 SCV001434533 likely benign Intellectual disability 2020-04-20 criteria provided, single submitter clinical testing

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