ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Personalized Diabetes Medicine Program, University of Maryland School of Medicine and "likely benign" from ClinGen Monogenic Diabetes Variant Curation Expert Panel

Minimum review status of the submission from Personalized Diabetes Medicine Program, University of Maryland School of Medicine: Collection method of the submission from Personalized Diabetes Medicine Program, University of Maryland School of Medicine:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP gnomAD frequency
NM_000545.8(HNF1A):c.142G>A (p.Glu48Lys) rs772222326 0.00009

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