ClinVar Miner

Submissions for variant NM_014550.4(CARD10):c.2485C>T (p.Arg829Trp)

gnomAD frequency: 0.00019  dbSNP: rs201794655
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Flinders Ophthalmology, Flinders University RCV000416608 SCV000266589 risk factor Primary open angle glaucoma 2016-03-29 no assertion criteria provided case-control GWAS associated gene CARD10

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