ClinVar Miner

Submissions for variant NM_012203.2(GRHPR):c.934A>G (p.Asn312Asp)

dbSNP: rs180177324
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV000186445 SCV004191721 likely pathogenic Primary hyperoxaluria, type II 2023-11-22 criteria provided, single submitter clinical testing
Clinical Biochemistry Laboratory, Health Services Laboratory RCV000186445 SCV000239800 pathogenic Primary hyperoxaluria, type II 2014-11-27 no assertion criteria provided in vitro

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