ClinVar Miner

Submissions for variant NM_020366.3(RPGRIP1):c.2896delG

dbSNP: rs863224913
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
UCLA Clinical Genomics Center, UCLA RCV000195884 SCV000255450 likely pathogenic Cone-rod dystrophy 13 2013-10-15 criteria provided, single submitter clinical testing

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