ClinVar Miner

Submissions for variant NM_015338.6(ASXL1):c.1181G>A (p.Arg394His)

gnomAD frequency: 0.00006  dbSNP: rs201899433
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002098640 SCV002397337 likely benign not provided 2025-01-16 criteria provided, single submitter clinical testing

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