ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.2381-46G>A (rs2072233)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000250374 SCV000316311 benign not specified criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001538011 SCV001754992 benign Usher syndrome, type 1C 2021-07-10 criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001538012 SCV001754993 benign Deafness, autosomal recessive 18 2021-07-10 criteria provided, single submitter clinical testing

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