SNPs associated with hypothyroidism at .

<p>All genomic positions are given with respect to NCBI build 36.3. Alleles are listed as major/minor and are specified for the forward strand. refers to the number of people successfully genotyped for each SNP. Odds ratios are per copy of the minor allele. One SNP is listed per region of the genome with the exception of HLA, which shows evidence of two independent signals, and <i>PTPN22</i>, for which we have included rs2476601, the non-synonymous change R620W.