SNP | Group | Genotype counts | p† | Rarer allele frequency | p‡ | ||
---|---|---|---|---|---|---|---|
1/1 | 1/2 | 2/2 | |||||
1/1, Homozygotes for the common variant; 1/2, heterozygotes; 2/2, homozygotes for the rare variant | |||||||
†p value for difference in genotype frequencies between probands and controls by Fisher’s exact test (1/2 and 2/2 grouped together) | |||||||
‡p value for difference in allele frequencies between probands and controls by Fisher’s exact test. | |||||||
R702W | CD | 21 | 9 | 0 | 0.007 | 0.15 | 0.01 |
UC | 46 | 8 | 0 | 0.46 | 0.07 | 0.47 | |
Controls | 96 | 11 | 1 | – | 0.06 | – | |
G908R | CD | 27 | 6 | 0 | 0.02 | 0.09 | 0.02 |
UC | 53 | 2 | 0 | 1 | 0.02 | 0.69 | |
Controls | 103 | 5 | 0 | – | 0.02 | – | |
L1007fsinsC | CD | 29 | 4 | 2 | 0.001 | 0.11 | 0.001 |
UC | 52 | 2 | 0 | 1 | 0.02 | 1 | |
Controls | 105 | 3 | 0 | – | 0.01 | – |