ClinVar Miner

Submissions for variant NM_033100.4(CDHR1):c.270dup (p.Thr91fs)

dbSNP: rs878853347
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
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 RCV000225405 SCV000282546 likely pathogenic Retinal dystrophy no assertion criteria provided clinical testing

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