ClinVar Miner

Submissions for variant NM_001613.4(ACTA2):c.370-19del

dbSNP: rs1554841385
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
Center for Human Genetics, Inc, Center for Human Genetics, Inc RCV000585753 SCV000693696 likely benign Connective tissue disorder 2015-12-31 criteria provided, single submitter clinical testing

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