ClinVar Miner

Submissions for variant NM_000169.3(GLA):c.237A>G (p.Glu79=)

dbSNP: rs2147480859
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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 RCV002091731 SCV002433949 likely benign Fabry disease 2022-04-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002091731 SCV004836043 likely benign Fabry disease 2023-11-20 criteria provided, single submitter clinical testing

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