ClinVar Miner

Submissions for variant NM_005027.4(PIK3R2):c.850G>A (p.Val284Met)

gnomAD frequency: 0.00001  dbSNP: rs1212577459
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Xiao lab, Department of Pathology, Memorial Sloan Kettering Cancer Center RCV000984112 SCV001132081 likely pathogenic Multiple myeloma 2019-08-31 no assertion criteria provided clinical testing

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