| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10824518 | 0.882 | 0.040 | 10 | 77303784 | intron variant | T/A;C | snv | 3 | |||
| rs1644731 | 0.925 | 0.040 | 19 | 10021323 | missense variant | T/A;C | snv | 4.0E-06; 0.52 | 2 | ||
| rs2233789 | 0.925 | 0.040 | 19 | 10013026 | upstream gene variant | C/A;T | snv | 2 | |||
| rs2973644 | 0.925 | 0.040 | 5 | 44384081 | intron variant | C/A;T | snv | 2 | |||
| rs3026393 | 0.925 | 0.040 | 11 | 31790667 | intron variant | A/C;G;T | snv | 0.48; 8.0E-06; 7.6E-05 | 2 | ||
| rs644242 | 0.882 | 0.040 | 11 | 31791253 | non coding transcript exon variant | C/A;G | snv | 3 | |||
| rs6885224 | 0.882 | 0.040 | 5 | 11169833 | intron variant | C/A;T | snv | 3 | |||
| rs747797174 | 0.925 | 0.040 | 15 | 74070978 | missense variant | C/A;G;T | snv | 1.2E-05 | 2 | ||
| rs79002828 | 0.925 | 0.040 | 5 | 44318015 | intron variant | A/G | snv | 9.6E-03 | 2 | ||
| rs3741834 | 0.925 | 0.040 | 12 | 91111607 | upstream gene variant | G/A | snv | 2.6E-02 | 2 | ||
| rs3759223 | 0.925 | 0.040 | 12 | 91113006 | upstream gene variant | A/G | snv | 2.7E-02 | 2 | ||
| rs12423791 | 0.925 | 0.040 | 12 | 102465050 | intron variant | G/C | snv | 2.8E-02 | 5 | ||
| rs17122571 | 0.925 | 0.040 | 12 | 48027251 | upstream gene variant | A/G | snv | 8.2E-02 | 2 | ||
| rs662702 | 0.882 | 0.040 | 11 | 31787522 | 3 prime UTR variant | C/T | snv | 0.15 | 3 | ||
| rs13382811 | 0.882 | 0.040 | 2 | 144466053 | intron variant | C/T | snv | 0.21 | 4 | ||
| rs5742632 | 0.851 | 0.120 | 12 | 102462696 | intron variant | A/G | snv | 0.26 | 4 | ||
| rs10860860 | 0.925 | 0.040 | 12 | 102387055 | non coding transcript exon variant | A/T | snv | 0.28 | 2 | ||
| rs4373767 | 0.882 | 0.040 | 1 | 219586340 | regulatory region variant | C/T | snv | 0.32 | 4 | ||
| rs10034228 | 0.882 | 0.040 | 4 | 111690594 | intergenic variant | T/C | snv | 0.32 | 3 | ||
| rs577948 | 0.882 | 0.040 | 11 | 122159482 | intron variant | A/G | snv | 0.33 | 3 | ||
| rs12716080 | 0.882 | 0.040 | 5 | 11166836 | intron variant | G/T | snv | 0.39 | 3 | ||
| rs6214 | 0.672 | 0.400 | 12 | 102399791 | 3 prime UTR variant | C/T | snv | 0.45 | 26 | ||
| rs7839488 | 0.882 | 0.040 | 8 | 120550178 | intron variant | G/A | snv | 0.47 | 4 | ||
| rs634990 | 0.827 | 0.040 | 15 | 34713872 | intergenic variant | T/C | snv | 0.48 | 6 | ||
| rs6469937 | 0.882 | 0.040 | 8 | 120598198 | intron variant | G/A | snv | 0.48 | 3 |