ClinVar Miner

Submissions for variant NM_198880.3(QRICH1):c.68C>T (p.Pro23Leu)

dbSNP: rs2106983539
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Goettingen RCV001391660 SCV001593281 likely pathogenic Ververi-Brady syndrome 2021-05-14 no assertion criteria provided clinical testing

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