ClinVar Miner

Submissions for variant NM_001854.4(COL11A1):c.3402G>A (p.Pro1134=)

gnomAD frequency: 0.00001  dbSNP: rs763588142
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 RCV000250090 SCV000308469 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001560487 SCV001782907 likely benign not provided 2020-01-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001560487 SCV003785157 benign not provided 2024-11-28 criteria provided, single submitter clinical testing

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