ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.2442G>A (p.Pro814=)

dbSNP: rs185808139
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001951650 SCV002241609 likely benign not provided 2024-10-08 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002497894 SCV002803769 likely benign Brachydactyly type B1; Autosomal recessive Robinow syndrome 2021-10-04 criteria provided, single submitter clinical testing

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