Fine mapping association results of <i>NRG1</i> SNPs using logistic regression on MACH-imputed allelic dosage

Only SNPs with P-value lower than either or both of the 2 previously implicated SNPs (rs16879552 and rs7835688) are shown; a: minor allele frequency; underlined: SNPs found associated in the previously reported GWAS. b: frequencies reported for imputed alleles (except for rs3802159 and rs7834206); c: minor and major alleles in patients and controls combined; in bold genotyped SNP with the lowest p association value.仅展示P值低于此前报道的2个关联单核苷酸多态性（Single Nucleotide Polymorphisms，SNPs）（rs16879552与rs7835688）其中之一或二者的位点； a：次要等位基因频率；下划线标注：此前发表的全基因组关联研究（Genome-Wide Association Study，GWAS）中鉴定出的关联SNPs。 b：推算等位基因的频率报道值（rs3802159与rs7834206除外）； c：患者与对照人群合并后的次要等位基因与主要等位基因；以粗体标注关联P值最低的已基因分型SNPs。