ClinVar Miner

Submissions for variant NM_001029883.3(PCARE):c.3264_3266del (p.Pro1089del)

dbSNP: rs138020654
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000079372 SCV000111242 benign not specified 2013-09-17 criteria provided, single submitter clinical testing
Invitae RCV000963259 SCV001110404 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003597962 SCV001157186 benign Retinitis pigmentosa 54 2023-11-08 criteria provided, single submitter clinical testing

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