ClinVar Miner

Submissions for variant NM_012203.2(GRHPR):c.598+1G>T

dbSNP: rs111256477
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000664698 SCV000788701 likely pathogenic Primary hyperoxaluria, type II 2016-12-28 criteria provided, single submitter clinical testing
Gharavi Laboratory, Columbia University RCV000723226 SCV000854357 uncertain significance not provided 2018-09-16 no assertion criteria provided research

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