ClinVar Miner

Submissions for variant NM_001851.6(COL9A1):c.876+77dup

dbSNP: rs34962262
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
GeneDx RCV001618869 SCV001844361 benign not provided 2019-08-11 criteria provided, single submitter clinical testing

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