ClinVar Miner

Submissions for variant NM_015629.4(PRPF31):c.945+2T>G

dbSNP: rs2146437002
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Goettingen RCV002246221 SCV002515933 likely pathogenic Retinitis pigmentosa 11 2022-03-21 criteria provided, single submitter clinical testing

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