ClinVar Miner

Submissions for variant NM_080680.3(COL11A2):c.1980C>T (p.Pro660=)

dbSNP: rs2229786
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000248982 SCV000315343 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000840664 SCV000982592 likely benign not provided 2020-12-07 criteria provided, single submitter clinical testing
Invitae RCV000840664 SCV002365212 benign not provided 2024-01-21 criteria provided, single submitter clinical testing

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