ClinVar Miner

Submissions for variant NM_015629.4(PRPF31):c.420+1G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Juno Genomics, Hangzhou Juno Genomics, Inc RCV004797417 SCV005416982 pathogenic Retinitis pigmentosa 11 criteria provided, single submitter clinical testing PM2_Supporting+PVS1+PP4

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