ClinVar Miner

Submissions for variant NM_005458.8(GABBR2):c.2413-3T>C

dbSNP: rs1830432060
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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 Wuerzburg RCV001328490 SCV001519645 uncertain significance Intellectual disability no assertion criteria provided clinical testing

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