| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11591741 | 1.000 | 0.080 | 10 | 100216744 | intron variant | G/C | snv | 0.30 | 1 | ||
| rs121912645 | 0.882 | 0.080 | 2 | 10048376 | missense variant | G/T | snv | 1.3E-04 | 8.4E-05 | 1 | |
| rs551238 | 0.925 | 0.160 | 7 | 100723905 | downstream gene variant | G/T | snv | 0.62 | 3 | ||
| rs72928364 | 1.000 | 0.080 | 3 | 100894935 | intron variant | C/T | snv | 0.39 | 2 | ||
| rs78900934 | 1.000 | 0.080 | 1 | 101272565 | upstream gene variant | C/A | snv | 0.32 | 1 | ||
| rs6598475 | 1.000 | 0.080 | 15 | 101446425 | intron variant | G/T | snv | 0.63 | 1 | ||
| rs6543087 | 1.000 | 0.080 | 2 | 101699471 | intron variant | A/G;T | snv | 1 | |||
| rs117168171 | 1.000 | 0.080 | 15 | 101854599 | downstream gene variant | C/G;T | snv | 2 | |||
| rs2607653 | 1.000 | 0.080 | 13 | 102066314 | intron variant | A/G | snv | 5.9E-02 | 2 | ||
| rs2548724 | 1.000 | 0.080 | 5 | 102284470 | intron variant | T/C | snv | 0.81 | 1 | ||
| rs6214 | 0.672 | 0.400 | 12 | 102399791 | 3 prime UTR variant | C/T | snv | 0.45 | 1 | ||
| rs972936 | 0.807 | 0.200 | 12 | 102431143 | intron variant | T/C | snv | 0.70 | 3 | ||
| rs4729854 | 1.000 | 0.080 | 7 | 102743216 | intron variant | T/A | snv | 0.35 | 1 | ||
| rs7729395 | 1.000 | 0.080 | 5 | 102764872 | intron variant | C/T | snv | 3.1E-02 | 2 | ||
| rs16869786 | 1.000 | 0.080 | 8 | 102777227 | regulatory region variant | T/C | snv | 1.4E-02 | 1 | ||
| rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 8 | |
| rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 2 | |
| rs4684677 | 0.742 | 0.360 | 3 | 10286769 | missense variant | T/A | snv | 0.10 | 6.6E-02 | 1 | |
| rs696217 | 0.662 | 0.640 | 3 | 10289773 | missense variant | G/T | snv | 8.8E-02 | 7.1E-02 | 2 | |
| rs72783884 | 1.000 | 0.080 | 5 | 102912212 | intron variant | A/T | snv | 6.8E-03 | 1 | ||
| rs12413409 | 0.790 | 0.200 | 10 | 102959339 | intron variant | G/A | snv | 9.0E-02 | 6 | ||
| rs78408340 | 1.000 | 0.080 | 5 | 103003035 | missense variant | C/G;T | snv | 3.7E-03; 8.1E-06 | 2 | ||
| rs35658696 | 1.000 | 0.080 | 5 | 103003107 | missense variant | A/G | snv | 3.1E-02 | 3.2E-02 | 3 | |
| rs7674212 | 1.000 | 0.080 | 4 | 103067742 | intron variant | G/A;T | snv | 1 | |||
| rs115505614 | 1.000 | 0.080 | 5 | 103087264 | 3 prime UTR variant | C/T | snv | 3.2E-02 | 1 |