ClinVar Miner

Submissions for variant NM_012203.1(GRHPR):c.866-25CT[9]

dbSNP: rs34302950
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241767 SCV000311879 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001709515 SCV001938801 benign not provided 2020-06-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001709515 SCV002446359 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneReviews RCV000186434 SCV000041225 benign Primary hyperoxaluria, type II 2011-05-05 no assertion criteria provided curation Converted during submission to Benign.
Clinical Biochemistry Laboratory, Health Services Laboratory RCV000186434 SCV000239786 uncertain significance Primary hyperoxaluria, type II 2014-11-27 no assertion criteria provided research

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