ClinVar Miner

Submissions for variant NM_012203.2(GRHPR):c.-4_-3delinsAT

dbSNP: rs796052077
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV000186437 SCV002813268 likely pathogenic Primary hyperoxaluria, type II 2021-10-14 criteria provided, single submitter clinical testing
Clinical Biochemistry Laboratory, Health Services Laboratory RCV000186437 SCV000239789 pathogenic Primary hyperoxaluria, type II 2014-11-27 no assertion criteria provided in vitro

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