ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.1645-2A>C

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dept Of Ophthalmology, Nagoya University RCV003890608 SCV004708057 pathogenic Retinal dystrophy 2023-10-01 criteria provided, single submitter research
Fulgent Genetics, Fulgent Genetics RCV005015083 SCV005641163 likely pathogenic Usher syndrome type 2A; Retinitis pigmentosa 39 2024-05-07 criteria provided, single submitter clinical testing

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