ClinVar Miner

Submissions for variant NM_001853.4(COL9A3):c.*9G>A

gnomAD frequency: 0.00986  dbSNP: rs116108376
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243188 SCV000308396 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001582820 SCV001813500 likely benign not provided 2022-06-03 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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