ClinVar Miner

Submissions for variant NM_014321.4(ORC6):c.257_258del (p.Ser85_Phe86insTer)

dbSNP: rs786205258
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Total submissions: 3
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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 RCV000023632 SCV000845235 pathogenic Meier-Gorlin syndrome 3 2018-08-07 criteria provided, single submitter clinical testing
Bicknell laboratory, University of Otago RCV000023632 SCV001738349 pathogenic Meier-Gorlin syndrome 3 criteria provided, single submitter research
OMIM RCV000023632 SCV000044923 pathogenic Meier-Gorlin syndrome 3 2011-02-27 no assertion criteria provided literature only

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