ClinVar Miner

Submissions for variant NM_000516.7(GNAS):c.873CAA[1] (p.Asn292del)

dbSNP: rs2091331588
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota RCV001289548 SCV001477500 likely pathogenic Pseudopseudohypoparathyroidism 2020-11-06 criteria provided, single submitter clinical testing

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