ClinVar Miner

Submissions for variant NM_000025.3(ADRB3):c.190T>C (p.Trp64Arg)

gnomAD frequency: 0.09116  dbSNP: rs4994
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001707510 SCV001935767 benign not provided 2021-06-09 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 9080262, 29670643, 22774474, 11380082, 21529759, 23729572, 21289629, 21358132, 20008926, 20069060, 11564599, 17225053, 19553224, 22550477, 19133996, 21285172, 21034552, 19080138, 7487991, 28456594, 23968135, 20078877, 23032405)
OMIM RCV000033197 SCV000057043 risk factor Obesity 2004-10-01 no assertion criteria provided literature only

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