Genomic risk loci for hearing difficulty.
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https://figshare.com/articles/dataset/Genomic_risk_loci_for_hearing_difficulty_/13016563
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资源简介：
Loci were defined by the set of all SNPs in LD (r2 > 0.6, 1000 Genomes Phase 3 European samples) with an independently significant SNP (p < 5e-8) at that locus. Start and end refer to the left- and rightmost positions of these SNPs (hg19 coordinates). nSNPs refers to the total number of SNPs in the locus, regardless of whether these SNPs were directly tested for association and included in the GWAS summary statistics. nGWASSNPs indicates the number of SNPs in the locus that were included in the GWAS summary statistics, a subset of "nSNPs". SNPs that are not in linkage disequilibrium with any of those identified in the previously published GWAS of hearing difficulty in the UK Biobank[9] are indicated in bold text.
(XLSX)
创建时间：
2020-09-28
