ClinVar Miner

Submissions for variant NM_015338.6(ASXL1):c.2387G>C (p.Trp796Ser)

gnomAD frequency: 0.00009  dbSNP: rs770674396
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000396645 SCV000338790 uncertain significance not provided 2016-01-08 criteria provided, single submitter clinical testing
GeneDx RCV000396645 SCV001871481 benign not provided 2020-01-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000396645 SCV002402392 benign not provided 2024-10-29 criteria provided, single submitter clinical testing

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