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Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.

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49articles
49mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

1 records shown · first 60
TypeEntitySource evidenceConfidenceExtractor
phenotypeendometrial cancer“Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.”0.98phenotype_alias_lexicon_v2
variantrs3184504“A combined analysis revealed one genome-wide significant polymorphism, rs3184504, on chromosome 12q24 (OR = 1.10, P = 7.23 × 10(-9)) with shared effects on CRC and EC risk.”0.90hgvs_regex_v1
geneSH2B3“Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.”0.98hgnc_dict_v1
geneTSHZ1“Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.”0.98hgnc_dict_v1