ClinVar Miner

Submissions for variant NM_002067.5(GNA11):c.95A>G (p.Asp32Gly)

dbSNP: rs200234790
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Cologne University RCV000857316 SCV000999915 uncertain significance Familial hypocalciuric hypercalcemia 2 no assertion criteria provided clinical testing

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