Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2237892 | 0.790 | 0.320 | 11 | 2818521 | intron variant | C/T | snv | 9.2E-02 | 2 | ||
| rs2237897 | 0.882 | 0.200 | 11 | 2837316 | intron variant | C/T | snv | 8.1E-02 | 2 | ||
| rs12576239 | 1.000 | 0.080 | 11 | 2481089 | intron variant | C/T | snv | 0.16 | 1 | ||
| rs163177 | 1.000 | 0.080 | 11 | 2817183 | intron variant | T/C | snv | 0.45 | 1 | ||
| rs163182 | 0.882 | 0.160 | 11 | 2822986 | intron variant | G/A;C | snv | 1 | |||
| rs163184 | 1.000 | 0.080 | 11 | 2825839 | intron variant | T/G | snv | 0.40 | 1 | ||
| rs2237895 | 0.790 | 0.240 | 11 | 2835964 | intron variant | A/C;T | snv | 1 | |||
| rs2237896 | 1.000 | 0.080 | 11 | 2837210 | intron variant | G/A;T | snv | 1 | |||
| rs2283228 | 1.000 | 0.080 | 11 | 2828300 | intron variant | A/C | snv | 0.10 | 1 | ||
| rs233449 | 1.000 | 0.080 | 11 | 2822573 | intron variant | G/A | snv | 0.22 | 1 | ||
| rs76868685 | 1.000 | 0.080 | 11 | 2836784 | intron variant | C/G | snv | 2.3E-04 | 1 | ||
| rs8181588 | 1.000 | 0.080 | 11 | 2810311 | intron variant | T/C | snv | 0.12 | 1 | ||
| rs77402029 | 1.000 | 0.080 | 11 | 2619190 | non coding transcript exon variant | G/A;T | snv | 1 | |||
| rs117601636 | 1.000 | 0.080 | 11 | 2620807 | non coding transcript exon variant | A/G | snv | 5.5E-03 | 1 | ||
| rs231356 | 0.925 | 0.080 | 11 | 2684113 | non coding transcript exon variant | A/G;T | snv | 1 | |||
| rs231361 | 1.000 | 0.080 | 11 | 2670270 | non coding transcript exon variant | G/A | snv | 0.31 | 1 | ||
| rs231362 | 1.000 | 0.080 | 11 | 2670241 | non coding transcript exon variant | A/G | snv | 0.62 | 1 |