ClinVar Miner

Submissions for variant NM_015338.6(ASXL1):c.2011G>T (p.Ala671Ser)

dbSNP: rs1600586513
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002118802 SCV002441500 likely benign not provided 2023-08-22 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002118802 SCV004152572 uncertain significance not provided 2022-11-01 criteria provided, single submitter clinical testing ASXL1: PM2, BP4

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