ClinVar Miner

Submissions for variant NC_000006.12:g.35506278_35506281del

dbSNP: rs2150925640
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
Genomics England Pilot Project, Genomics England RCV001542665 SCV001760179 pathogenic Retinitis pigmentosa 14 no assertion criteria provided clinical testing

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