SNP | Chr: position (Build 38) | Reference position* | Major/minor allele | Risk allele | Cases | Controls | OR (95% CI) | Pvalue (empiricalPvalue) | OR (95% CI)§ | Pvalue§ | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|
(n = 593) | (n = 388) | |||||||||||
 |  |  |  |  | Minor allele frequencies | Genotype count 11/12/22# | Minor allele frequencies | Genotype count 11/12/22# |  |  |  |  |
rs2808629 | 1:159707006 | +5283 | A/G | G | 0.452 | 171/297/115 | 0.389 | 141/180/57 | 1.296(1.076,1.561) | 0.006(0.029) | 1.261(1.022,1.555) | 0.030 |
rs3093077 | 1:159709846 | +2443 | T/G | G | 0.183 | 390/179/18 | 0.163 | 271/106/10 | 1.153(0.906,1.468) | 0.248(0.612) | 1.194(0.906,1.574) | 0.209 |
rs1130864 | 1:159713301 | 3’ UTR | C/T | T | 0.058 | 520/62/3 | 0.045 | 352/33/1 | 1.299(0.855,1.974) | 0.219(0.667) | 1.250(0.794,1.968) | 0.335 |
rs2808634 | 1:159722783 | −8194 | C/T | T | 0.160 | 420/155/17 | 0.151 | 281/97/10 | 1.070(0.833,1.375) | 0.597(0.968) | 1.056(0.804,1.386) | 0.697 |