ClinVar Miner

Submissions for variant NM_002292.4(LAMB2):c.5258dup (p.Glu1754fs)

dbSNP: rs1560063136
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000015630 SCV000035895 pathogenic Pierson syndrome 2004-11-01 no assertion criteria provided literature only

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