ClinVar Miner

Submissions for variant NM_002906.4(RDX):c.1587+38T>G

gnomAD frequency: 0.41780  dbSNP: rs10450619
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001680404 SCV001898034 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796697 SCV002033487 benign Autosomal recessive nonsyndromic hearing loss 24 2021-11-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001680404 SCV005231537 benign not provided criteria provided, single submitter not provided

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