ClinVar Miner

Submissions for variant NM_002067.5(GNA11):c.189C>T (p.His63=)

gnomAD frequency: 0.00108  dbSNP: rs61731116
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000245319 SCV000308691 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000886037 SCV001029520 benign not provided 2024-01-04 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000245319 SCV002065587 benign not specified 2021-06-21 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000245319 SCV002552050 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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