ClinVar Miner

Submissions for variant NM_000883.4(IMPDH1):c.809T>G (p.Leu270Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dept Of Ophthalmology, Nagoya University RCV003891151 SCV004704795 likely pathogenic Retinal dystrophy 2023-10-01 criteria provided, single submitter research

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