ClinVar Miner

Submissions for variant NM_001032221.6(STXBP1):c.876C>A (p.Arg292=)

dbSNP: rs778838622
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 RCV000999214 SCV001155730 uncertain significance not provided 2016-05-01 criteria provided, single submitter clinical testing

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