ClinVar Miner

Submissions for variant NM_005012.4(ROR1):c.1353A>G (p.Val451=)

gnomAD frequency: 0.32509  dbSNP: rs6668545
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Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001669538 SCV001887431 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796673 SCV002033666 benign Hearing loss, autosomal recessive 108 2021-11-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001669538 SCV002478660 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001669538 SCV005287327 benign not provided criteria provided, single submitter not provided

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