ClinVar Miner

Submissions for variant NM_004153.4(ORC1):c.1482-2A>G

dbSNP: rs1378348220
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000023159 SCV000044450 pathogenic Meier-Gorlin syndrome 1 2011-02-27 no assertion criteria provided literature only

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