ClinVar Miner

Submissions for variant NM_001378414.1(HDAC4):c.565C>T (p.Arg189Trp)

dbSNP: rs746764988
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 RCV001260718 SCV001437810 likely benign Intellectual disability 2020-09-10 criteria provided, single submitter clinical testing

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