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Association of genetic variants in BCL-2-family genes with endometrial cancer risk among 1,028 cases and 1,922 controls, the Shanghai Endometrial Cancer Genetics Study (SECGS).

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Figshare2015-12-02 更新2026-04-29 收录
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https://figshare.com/articles/dataset/_Association_of_genetic_variants_in_BCL_2_family_genes_with_endometrial_cancer_risk_among_1_028_cases_and_1_922_controls_the_Shanghai_Endometrial_Cancer_Genetics_Study_SECGS_/689340
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aMajor/minor alleles.bMinor allele frequency in controls.cAdjusted for age and education. SNPs associated with endometrial cancer risk (P valueP values were not corrected for multiple tests.Notes:-AA indicates homozygotes for the major allele, who were used as the reference group (not shown in the table), Aa indicates heterozygotes and aa indicates homozygotes for the minor allele.-No deviation from Hardy-Weinberg Equilibrium (HWE) was observed for any given SNP among controls.-5UTR, 5′ untranslated region; 3′ UTR, 3′ untranslated region.-Significant SNPs are presented in bold.
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2015-12-02
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