| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17028719 | 1.000 | 0.080 | 1 | 5734948 | intergenic variant | A/G | snv | 4.8E-02 | 1 | ||
| rs17616845 | 1.000 | 0.080 | 7 | 12741918 | intron variant | T/C | snv | 0.15 | 1 | ||
| rs1995364 | 1.000 | 0.080 | 5 | 10903669 | intergenic variant | A/G | snv | 0.62 | 1 | ||
| rs2727943 | 0.925 | 0.080 | 3 | 1856289 | intergenic variant | T/A;C | snv | 1 | |||
| rs4384980 | 1.000 | 0.080 | 3 | 182741281 | upstream gene variant | A/C | snv | 0.48 | 1 | ||
| rs4610908 | 1.000 | 0.080 | X | 35166418 | intergenic variant | G/A | snv | 0.24 | 1 | ||
| rs6425323 | 1.000 | 0.080 | 1 | 175155900 | downstream gene variant | C/T | snv | 0.39 | 1 | ||
| rs7607774 | 1.000 | 0.080 | 2 | 236520511 | intergenic variant | G/A | snv | 7.4E-02 | 1 | ||
| rs7777391 | 1.000 | 0.080 | 7 | 117981823 | intergenic variant | A/G | snv | 0.60 | 1 | ||
| rs9847462 | 1.000 | 0.080 | 3 | 164840807 | intergenic variant | A/G | snv | 0.14 | 1 | ||
| rs994029 | 1.000 | 0.080 | 9 | 86760399 | downstream gene variant | C/T | snv | 0.71 | 1 | ||
| rs12006002 | 1.000 | 0.080 | 9 | 18166901 | intron variant | C/T | snv | 0.30 | 1 | ||
| rs6943555 | 0.882 | 0.080 | 7 | 70341037 | intron variant | T/A | snv | 0.34 | 1 | ||
| rs10913569 | 1.000 | 0.080 | 1 | 178548873 | non coding transcript exon variant | A/G;T | snv | 1 | |||
| rs29230 | 0.807 | 0.440 | 6 | 29608616 | missense variant | A/C;G | snv | 4.1E-06; 0.18 | 1 | ||
| rs279871 | 0.882 | 0.080 | 4 | 46303716 | intron variant | T/C | snv | 0.38 | 1 | ||
| rs6060124 | 1.000 | 0.080 | 20 | 34949094 | intron variant | C/A | snv | 0.27 | 1 | ||
| rs4935356 | 1.000 | 0.080 | 6 | 32444611 | intron variant | T/A;G | snv | 1 | |||
| rs1057302 | 1.000 | 0.080 | 1 | 175157287 | 3 prime UTR variant | A/G | snv | 0.38 | 1 | ||
| rs12901215 | 1.000 | 0.080 | 15 | 38700692 | intron variant | G/A | snv | 0.24 | 1 | ||
| rs12903120 | 1.000 | 0.080 | 15 | 38695896 | intron variant | G/T | snv | 0.26 | 1 | ||
| rs12916379 | 1.000 | 0.080 | 15 | 38699319 | non coding transcript exon variant | A/G | snv | 0.22 | 1 | ||
| rs2132157 | 1.000 | 0.080 | 15 | 38700346 | intron variant | A/G | snv | 0.25 | 1 | ||
| rs2172835 | 1.000 | 0.080 | 15 | 38697970 | intron variant | C/G;T | snv | 1 | |||
| rs34141940 | 1.000 | 0.080 | 15 | 38697456 | intron variant | G/A | snv | 0.25 | 1 |