ClinVar Miner

Submissions for variant NM_004048.4(B2M):c.286G>A (p.Asp96Asn)

dbSNP: rs398122820
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000989305 SCV001139577 pathogenic Non-Hodgkin lymphoma 2019-05-28 criteria provided, single submitter clinical testing
OMIM RCV000024598 SCV000045907 pathogenic Familial visceral amyloidosis, Ostertag type 2012-06-14 no assertion criteria provided literature only

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