ClinVar Miner

Submissions for variant NM_012203.2(GRHPR):c.867_870dup (p.Leu291fs)

dbSNP: rs1554749639
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000673697 SCV000798930 uncertain significance Primary hyperoxaluria, type II 2018-03-30 criteria provided, single submitter clinical testing
Baylor Genetics RCV000673697 SCV004191724 likely pathogenic Primary hyperoxaluria, type II 2023-03-04 criteria provided, single submitter clinical testing

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