| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3818753 | 1.000 | 0.200 | 1 | 64873549 | 3 prime UTR variant | A/G | snv | 1.0E-02 | 3.6E-03 | 3 | |
| rs4073153 | 1.000 | 0.200 | 9 | 136364897 | non coding transcript exon variant | A/G | snv | 0.40 | 3 | ||
| rs10236188 | 1.000 | 0.200 | 7 | 150548168 | intergenic variant | T/C | snv | 0.49 | 1 | ||
| rs10256482 | 1.000 | 0.200 | 7 | 150653887 | intergenic variant | T/C | snv | 0.47 | 1 | ||
| rs10277380 | 1.000 | 0.200 | 7 | 150533604 | intergenic variant | T/A;C | snv | 1 | |||
| rs10454134 | 1.000 | 0.200 | 2 | 48420887 | TF binding site variant | G/A | snv | 0.14 | 1 | ||
| rs1057519328 | 1.000 | 0.200 | 16 | 3249592 | missense variant | G/C | snv | 2.1E-05 | 1 | ||
| rs1065407 | 1.000 | 0.200 | 5 | 96776379 | 3 prime UTR variant | T/A;G | snv | 3.3E-05; 0.26 | 1 | ||
| rs111874856 | 1.000 | 0.200 | 18 | 21028924 | missense variant | C/T | snv | 1 | |||
| rs112108028 | 1.000 | 0.200 | 18 | 20959861 | missense variant | G/A | snv | 1 | |||
| rs112130712 | 1.000 | 0.200 | 18 | 20967783 | missense variant | T/C | snv | 1 | |||
| rs11574944 | 1.000 | 0.200 | 16 | 30498669 | intron variant | C/T | snv | 0.25 | 1 | ||
| rs116799036 | 1.000 | 0.200 | 6 | 31381371 | downstream gene variant | G/A | snv | 1 | |||
| rs11769828 | 1.000 | 0.200 | 7 | 150534221 | intergenic variant | C/T | snv | 0.19 | 1 | ||
| rs12141431 | 1.000 | 0.200 | 1 | 67281340 | downstream gene variant | G/C | snv | 0.23 | 1 | ||
| rs13154629 | 1.000 | 0.200 | 5 | 96786754 | non coding transcript exon variant | C/T | snv | 0.16 | 1 | ||
| rs1327295035 | 1.000 | 0.200 | 6 | 52187730 | missense variant | A/G | snv | 1 | |||
| rs1462891 | 1.000 | 0.200 | 8 | 31973417 | intron variant | T/C | snv | 0.72 | 1 | ||
| rs146597836 | 1.000 | 0.200 | 22 | 17189987 | missense variant | C/T | snv | 1.8E-03 | 1.6E-03 | 1 | |
| rs149034313 | 1.000 | 0.200 | 22 | 31278338 | missense variant | C/G;T | snv | 6.4E-03; 1.2E-05 | 1 | ||
| rs1522596 | 1.000 | 0.200 | 7 | 150538695 | downstream gene variant | A/G | snv | 0.47 | 1 | ||
| rs1608157 | 1.000 | 0.200 | 7 | 150549936 | intergenic variant | C/G;T | snv | 1 | |||
| rs17006292 | 1.000 | 0.200 | 2 | 121261187 | intron variant | C/A | snv | 2.8E-02 | 1 | ||
| rs17633132 | 1.000 | 0.200 | 8 | 17642610 | splice region variant | C/G;T | snv | 8.0E-06; 0.11 | 1 | ||
| rs1916012 | 1.000 | 0.200 | 7 | 150536739 | intergenic variant | A/G | snv | 0.49 | 1 |