ClinVar Miner

Submissions for variant NM_012203.2(GRHPR):c.954_955del (p.Glu320fs)

dbSNP: rs1554749672
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000666802 SCV000791158 uncertain significance Primary hyperoxaluria, type II 2017-05-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001532161 SCV001747590 likely pathogenic not provided 2021-03-01 criteria provided, single submitter clinical testing

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