| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
| rs895819 | 0.623 | 0.560 | 19 | 13836478 | non coding transcript exon variant | T/A;C;G | snv | 0.34 | 0.38 | 46 | |
| rs17860508 | 0.752 | 0.360 | 5 | 159333192 | intron variant | TTAGAG/GC | delins | 11 | |||
| rs76980269 | 0.763 | 0.280 | 12 | 117330794 | synonymous variant | G/A | snv | 2.8E-05 | 4.2E-05 | 10 | |
| rs4962153 | 0.925 | 0.120 | 9 | 133458632 | intron variant | A/G | snv | 0.79 | 9 | ||
| rs1478604 | 0.807 | 0.240 | 15 | 39581120 | 5 prime UTR variant | T/C | snv | 0.40 | 9 | ||
| rs2257167 | 0.807 | 0.200 | 21 | 33343393 | missense variant | G/C | snv | 0.18 | 0.16 | 7 | |
| rs41297579 | 0.807 | 0.280 | 5 | 157059397 | upstream gene variant | C/T | snv | 0.15 | 6 | ||
| rs2227473 | 0.851 | 0.160 | 12 | 68255258 | upstream gene variant | C/T | snv | 0.20 | 6 | ||
| rs56061981 | 0.851 | 0.120 | 4 | 76023632 | intron variant | C/T | snv | 7.6E-02 | 5 | ||
| rs5368 | 0.882 | 0.160 | 1 | 169727805 | missense variant | G/A | snv | 0.14 | 0.11 | 4 | |
| rs4508917 | 0.882 | 0.160 | 4 | 76024944 | intron variant | A/G | snv | 0.29 | 3 | ||
| rs2073342 | 0.882 | 0.200 | 14 | 20892057 | missense variant | C/G | snv | 0.73 | 0.65 | 3 | |
| rs2233860 | 0.882 | 0.160 | 14 | 20892185 | 3 prime UTR variant | G/C | snv | 0.18 | 0.19 | 3 | |
| rs9429942 | 0.925 | 0.080 | 1 | 207495285 | upstream gene variant | C/T | snv | 0.64 | 2 | ||
| rs8019343 | 0.925 | 0.080 | 14 | 20892263 | 3 prime UTR variant | A/T | snv | 4.2E-02 | 2 | ||
| rs4715291 | 1.000 | 0.080 | 6 | 52248562 | upstream gene variant | C/A;T | snv | 1 | |||
| rs6913472 | 1.000 | 0.080 | 6 | 52232274 | downstream gene variant | G/A | snv | 8.2E-02 | 1 | ||
| rs41297577 | 1.000 | 0.080 | 5 | 157059492 | upstream gene variant | C/A;G;T | snv | 1 | |||
| rs7702919 | 1.000 | 0.080 | 5 | 157059580 | upstream gene variant | T/C | snv | 0.56 | 1 | ||
| rs1041867 | 1.000 | 0.080 | 21 | 33354946 | intron variant | T/G | snv | 0.48 | 1 | ||
| rs12626750 | 1.000 | 0.080 | 21 | 33326080 | intron variant | C/A | snv | 0.24 | 1 | ||
| rs914142 | 1.000 | 0.080 | 21 | 33353501 | intron variant | G/A;T | snv | 1 | |||
| rs139262191 | 1.000 | 0.080 | 9 | 21077768 | missense variant | G/C;T | snv | 7.0E-04; 4.2E-04; 4.0E-06 | 1 | ||
| rs12159217 | 1.000 | 0.080 | 22 | 17093025 | intron variant | G/T | snv | 0.11 | 1 |