ClinVar Miner

Submissions for variant NM_017831.4(RNF125):c.318+23T>G

gnomAD frequency: 0.72867  dbSNP: rs9947278
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001794906 SCV002033647 benign Tenorio syndrome 2021-11-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711716 SCV005247237 benign not provided criteria provided, single submitter not provided

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