ClinVar Miner

Submissions for variant NM_012203.2(GRHPR):c.457C>T (p.Gln153Ter)

dbSNP: rs1341484544
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV001264364 SCV001442468 likely pathogenic Primary hyperoxaluria, type II 2019-09-26 criteria provided, single submitter clinical testing

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