ClinVar Miner

Submissions for variant NM_004153.4(ORC1):c.1964C>T (p.Thr655Ile)

dbSNP: rs1569920188
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000791113 SCV000930387 uncertain significance Meier-Gorlin syndrome 1 2019-04-27 criteria provided, single submitter clinical testing

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