ClinVar Miner

Submissions for variant NM_003011.4(SET):c.701A>G (p.Glu234Gly)

gnomAD frequency: 0.00001  dbSNP: rs768759521
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Donald Williams Parsons Laboratory, Baylor College of Medicine RCV000505665 SCV000599954 other Hepatocellular carcinoma 2016-05-01 no assertion criteria provided clinical testing

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