ClinVar Miner

Submissions for variant NM_001851.6(COL9A1):c.975+45G>A

gnomAD frequency: 0.21907  dbSNP: rs7764822
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000249345 SCV000308354 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001675713 SCV001893040 benign not provided 2018-06-26 criteria provided, single submitter clinical testing

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