ClinVar Miner

Submissions for variant NM_006343.3(MERTK):c.584-1G>T

dbSNP: rs1553449458
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000502117 SCV000588383 pathogenic Retinitis pigmentosa 38 2020-05-03 criteria provided, single submitter clinical testing

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