Table 2.
Chr | Marker | Position a | Gene | Marker Information | |||
---|---|---|---|---|---|---|---|
Alleles b | MAF c | HW p-Value | %Genotyping | ||||
4 | rs1565902 | 61,542,902 | ADGRL3 | C/T | 0.473 | 0.048 | 89.4 |
4 | rs10001410 | 61,608,511 | ADGRL3 | C/T | 0.372 | 0.841 | 92.0 |
4 | rs2122642 | 61,832,546 | ADGRL3 | C/T | 0.330 | 0.326 | 91.5 |
5 | rs2282794 | 142,602,144 | FGF1 | G/A | 0.458 | 0.244 | 85.8 |
11 | rs916457 | 637,014 | DRD4 | C/A | 0.074 | 0.546 | 88.1 |
20 | rs362990 | 10,295,573 | SNAP25 | T/G | 0.120 | 0.788 | 80.3 |
a UCSC GRCh37/hg19 coordinates. b Minor allele reported in bold. c Sample-based estimate. Chr: Chromosome; MAF: Minor allele frequency; HW: Hardy–Weinberg. Additional details on these intronic markers are provided in Table S1. Note: The p-value for the HW disequilibrium test was calculated for the full sample.