ClinVar Miner

Submissions for variant NM_145290.4(ADGRA3):c.858C>T (p.Thr286=)

dbSNP: rs35762546
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001513630 SCV001721279 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Dept Of Ophthalmology, Nagoya University RCV003888251 SCV004706534 benign Retinal dystrophy 2023-10-01 criteria provided, single submitter research
Breakthrough Genomics, Breakthrough Genomics RCV001513630 SCV005298887 benign not provided criteria provided, single submitter not provided

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