ClinVar Miner

Submissions for variant NM_005012.4(ROR1):c.1170G>T (p.Ala390=)

gnomAD frequency: 1.00000  dbSNP: rs2762833
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001698907 SCV001916828 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001794491 SCV002033665 benign Hearing loss, autosomal recessive 108 2021-11-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001698907 SCV002436678 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001698907 SCV005287322 benign not provided criteria provided, single submitter not provided

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