ClinVar Miner

Submissions for variant NM_133171.5(ELMO2):c.1279+19del

dbSNP: rs76979752
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001650545 SCV001870591 benign not provided 2021-05-12 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501996 SCV002810744 likely benign Primary intraosseous venous malformation 2021-11-12 criteria provided, single submitter clinical testing

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