Genomic Co-occurrence
Analysis Portal

DNMT3A R882H · IDH2 R140Q · SETBP1 G870S · PTPN11 E76Q · EZH2 V662A
Monosomy 7
0 matches in 31,000+ myeloid patients (GENIE v19.0).
Pairwise-corrected expected frequency: 1 in 1.9 billion.
🇮🇹
Dr. Rocco Piazza
University of Milano-Bicocca
SETBP1 co-occurrence, population-level statistics
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🇯🇵
Dr. Hideki Makishima
Shinshu University
DDX41, SETBP1 SKI domain, rare myeloid variants
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How to cite
Kroine HG. Genomics Researcher Portal. The Educational Equality Institute; 2026.
This portal is password-protected. If you received a link and cannot access the research pages, contact henrik@theeducationalequalityinstitute.org to request access.
Independent patient-driven genomic analysis · GENIE v19.0
Built with Claude Code · 2026