ClinVar Miner

Submissions for variant NM_015338.6(ASXL1):c.2324T>C (p.Leu775Ser)

dbSNP: rs752263134
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001970448 SCV002255541 benign not provided 2022-08-23 criteria provided, single submitter clinical testing

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