ClinVar Miner

Submissions for variant NM_000273.3(GPR143):c.767+10C>G

dbSNP: rs3788938
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000249929 SCV000303411 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001511112 SCV001718301 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701955 SCV001933908 benign Nystagmus 6, congenital, X-linked 2021-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701887 SCV001933909 benign Ocular albinism, type I 2021-08-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001511112 SCV005279082 benign not provided criteria provided, single submitter not provided

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