ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.51C>A (p.Ala17=)

gnomAD frequency: 0.00003  dbSNP: rs886043361
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000395548 SCV000339663 uncertain significance not provided 2016-03-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000395548 SCV002418766 likely benign not provided 2024-11-18 criteria provided, single submitter clinical testing

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