ClinVar Miner

Submissions for variant NM_022489.4(INF2):c.353T>A (p.Ile118Asn)

dbSNP: rs2140639518
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Yale Center for Mendelian Genomics, Yale University RCV001849669 SCV002106621 likely pathogenic Focal segmental glomerulosclerosis 5 2019-02-14 no assertion criteria provided literature only

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