ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Department of Hematology - Research Laboratory 1, Postgraduate Institute of Medical Education and Research and "pathogenic" from any submitter

Minimum review status of the submission from Department of Hematology - Research Laboratory 1, Postgraduate Institute of Medical Education and Research: Collection method of the submission from Department of Hematology - Research Laboratory 1, Postgraduate Institute of Medical Education and Research:
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_001754.5(RUNX1):c.679G>T (p.Glu227Ter) rs1555889984

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