ClinVar Miner

Submissions for variant NM_001034853.2(RPGR):c.908G>A (p.Gly303Glu)

dbSNP: rs878853375
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Genomic Medicine, Manchester, Central Manchester University Hospitals RCV000225387 SCV000282589 uncertain significance Retinal dystrophy no assertion criteria provided clinical testing
Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg RCV000225387 SCV005069994 uncertain significance Retinal dystrophy 2022-01-01 no assertion criteria provided clinical testing

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