ClinVar Miner

Submissions for variant NM_033031.3(CCNB3):c.3752T>A (p.Val1251Asp)

dbSNP: rs1602253764
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Academic Center for Education, Culture and Research, Motamed Cancer Institute RCV000824808 SCV000886503 pathogenic Pregnancy loss, recurrent, susceptibility to, 1 no assertion criteria provided research

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