ClinVar Miner

Submissions for variant NM_000754.4(COMT):c.597G>A (p.Pro199=)

gnomAD frequency: 0.04486  dbSNP: rs769224
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001595064 SCV001828215 benign not provided 2021-05-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001595064 SCV005275354 benign not provided criteria provided, single submitter not provided
Bruce Budowle Laboratory, University of North Texas Health Science Center RCV001028870 SCV001191656 drug response Tramadol response 2018-04-28 no assertion criteria provided research

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