ClinVar Miner

Submissions for variant NM_177924.5(ASAH1):c.126-7A>G

dbSNP: rs771021569
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Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002188306 SCV002484064 likely benign not provided 2025-02-02 criteria provided, single submitter clinical testing
Athena Diagnostics RCV002188306 SCV002770790 uncertain significance not provided 2022-01-31 criteria provided, single submitter clinical testing

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