Appendix 1 of Musolf, Mol Vis 2018; 24:29-42.

Appendix 1. Genome-wide Suggestive Variants from Single Variant Two-point Analysis

Table displaying the genome-wide significant and suggestive linkage signals from the single variant two-point linkage analysis sorted by HLOD. The genome-wide significance threshold is 3.3 and the genome-wide suggestive threshold is 1.9, as recommended by Lander and Kruglyak. CHR=chromosomal region, HLOD=heterogeneity LOD score, POS=position in basepairs of the SNP, MAF=minor allele frequency as calculated from the data set, FUNCTION=functional annotation of the SNP, GENE=genic location of the SNP or closest genes in the case of intergenic SNPs. Annotations performed by ANNOVAR. To access the data, click or select the words “Appendix 1