ClinVar Miner

Submissions for variant NM_022370.4(ROBO3):c.766+24T>C

gnomAD frequency: 0.62538  dbSNP: rs4936957
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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 RCV001794911 SCV002033657 benign Gaze palsy, familial horizontal, with progressive scoliosis 1 2021-11-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004709165 SCV005231030 benign not provided criteria provided, single submitter not provided

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