Genome-wide association statistics of Hearing Problems

Genome-wide Association Statistics of Hearing Problems Citation: De Angelis F, Zeleznik OA, Wendt FR, Pathak GA, Tylee DS, De Lillo A, Koller D, Cabrera-Mendoza B, Clifford RE, Maihofer AX, Nievergelt CM, Curhan GC, Curhan SG, Polimanti R. Sex differences in the polygenic architecture of hearing problems in adults. Genome Med. https://doi.org/10.1186/s13073-023-01186-3 COLUMN HEADERS<br> chromosome: chromosome<br> base_pair_location: position<br> effect_allele: effect allele (corresponds to the effect size’s sign; may not be the alternate allele)<br> other_allele: non-effect allele<br> beta: effect measured as beta, sign corresponds to the effect of the effect allele<br> standard_error: standard error of the effect<br> effect_allele_frequency: effect allele frequency in UK Biobank participants of European descent<br> p_value: p value of the association statistic<br> variant_id: variant identifier<br> rs_id: rsID of the variant<br> n: sample size per variant