ClinVar Miner

Submissions for variant NM_012301.4(MAGI2):c.3998del (p.Gly1333fs)

dbSNP: rs1135402911
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000497254 SCV000588864 pathogenic Nephrotic syndrome 15 2018-07-18 no assertion criteria provided literature only

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