ClinVar Miner

Submissions for variant NM_002906.4(RDX):c.-64-6del

dbSNP: rs61003001
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV004577808 SCV000367176 likely benign Hearing loss, autosomal recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001718612 SCV000717168 benign not provided 2018-06-08 criteria provided, single submitter clinical testing
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital RCV001731577 SCV001984253 benign Autosomal recessive nonsyndromic hearing loss 24 2020-02-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001731577 SCV002033488 benign Autosomal recessive nonsyndromic hearing loss 24 2021-11-07 criteria provided, single submitter clinical testing

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