ClinVar Miner

Submissions for variant NM_022489.4(INF2):c.161G>C (p.Arg54Pro)

dbSNP: rs866348422
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota RCV001261441 SCV001438738 likely pathogenic Focal segmental glomerulosclerosis 5 2020-05-13 criteria provided, single submitter clinical testing

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