PMC:4564992 / 67880-68781 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/4564992","sourcedb":"PMC","sourceid":"4564992","source_url":"https://www.ncbi.nlm.nih.gov/pmc/4564992","text":"Shown are the results at the five SNPs on chromosomes 12 and 13 with the lowest p values, when using EMIM with and without haplotype estimation. Cell counts are shown for the ambiguous scenarios in which all individuals are heterozygous: cell 9 for case-parent trios and cell 4 for case-mother duos and case-father duos. The estimated number of trios and duos in which the risk allele is inherited from the father is given as cells 9a and 4a, respectively, and the estimated number in which the risk allele is inherited from the mother is given as cells 9b and 4b, respectively. Cell counts estimated from duos need not be integers given that they incorporate the adjustment described in Appendix B. The odds ratios and p values given by EMIM, with and without haplotype estimation, are shown. Chromosomes 12 and 13 were tested for paternally and maternally inherited imprinting effects, respectively.","tracks":[]}