ClinVar Miner

Submissions for variant NM_001853.4(COL9A3):c.1107+1G>C

dbSNP: rs1384292566
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eye Genetics Research Group, Children's Medical Research Institute RCV001283725 SCV001424845 likely pathogenic Retinal detachment; Lattice retinal degeneration 2020-07-22 no assertion criteria provided clinical testing

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