ClinVar Miner

Submissions for variant NM_000754.4(COMT):c.289+90A>G

gnomAD frequency: 0.39046  dbSNP: rs2239393
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001673008 SCV001883355 benign not provided 2021-05-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001673008 SCV005275348 benign not provided criteria provided, single submitter not provided
Bruce Budowle Laboratory, University of North Texas Health Science Center RCV001029702 SCV001192488 drug response Tramadol response 2018-04-28 no assertion criteria provided research

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