ClinVar Miner

Submissions for variant NM_001854.4(COL11A1):c.4033-10C>T

gnomAD frequency: 0.00001  dbSNP: rs763204252
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001704541 SCV000534025 likely benign not provided 2020-09-11 criteria provided, single submitter clinical testing
Invitae RCV001704541 SCV002941183 likely benign not provided 2023-08-27 criteria provided, single submitter clinical testing

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