ClinVar Miner

Submissions for variant NM_145343.2(APOL1):c.1072A>G (p.Ser358Gly) (rs73885319)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000408955 SCV000204327 not provided Focal segmental glomerulosclerosis 4, susceptibility to 2014-12-09 no assertion provided clinical testing

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