Table 2.
SNP ID | CHR* | Position | Odds Ratio* | 95% CI | P-value* | Reference allele | Effect allele | EAF* | Gene symbol | |
---|---|---|---|---|---|---|---|---|---|---|
Lower boundary | Upper boundary | |||||||||
rs380286** | 5 | 1320247 | 0.770 | 0.723 | 0.820 | 4.32×10−16 | A | G | 0.4169 | CLPTM1L |
rs31490† | 5 | 1344458 | 0.769 | 0.722 | 0.820 | 5.31×10−16 | G | A | 0.4142 | CLPTM1L |
rs4975616‡ | 5 | 1315660 | 0.778 | 0.730 | 0.829 | 1.04×10−14 | G | A | 0.4005 | CLPTM1L |
Adjusted for age, gender, and the first 5 principal components; CHR, chromosome; EAF, effect allele frequency
intronic variant
splice variant
downstream gene variant