ClinVar Miner

Submissions for variant NM_000169.3(GLA):c.174A>G (p.Glu58=)

dbSNP: rs2147487025
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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 RCV001427134 SCV001629807 likely benign Fabry disease 2019-06-25 criteria provided, single submitter clinical testing

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