ClinVar Miner

Submissions for variant NM_174878.3(CLRN1):c.98G>A (p.Trp33Ter)

dbSNP: rs878853379
Minimum review status: Collection method:
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Total submissions: 1
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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 RCV000225684 SCV000282597 likely pathogenic Retinal dystrophy no assertion criteria provided clinical testing

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