ClinVar Miner

Submissions for variant NM_001854.4(COL11A1):c.275-17del

dbSNP: rs3841819
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000254324 SCV000308461 likely benign not specified criteria provided, single submitter clinical testing
Center for Human Genetics, Inc, Center for Human Genetics, Inc RCV000659305 SCV000781116 likely benign Connective tissue disorder 2016-11-01 criteria provided, single submitter clinical testing
Invitae RCV002058090 SCV002406650 benign not provided 2023-12-26 criteria provided, single submitter clinical testing

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