| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11124945 | 1.000 | 0.040 | 2 | 43650017 | intron variant | A/G | snv | 0.21 | 3 | ||
| rs113296370 | 1.000 | 0.040 | 2 | 43636315 | upstream gene variant | A/C | snv | 0.17 | 3 | ||
| rs12632110 | 1.000 | 0.080 | 3 | 50186792 | intron variant | A/G | snv | 0.63 | 0.62 | 3 | |
| rs147783135 | 1.000 | 0.080 | 3 | 112081004 | stop gained | C/T | snv | 2.4E-04 | 6.3E-05 | 3 | |
| rs191885206 | 1.000 | 0.080 | 19 | 15696024 | missense variant | T/C | snv | 7.0E-04 | 3.1E-04 | 3 | |
| rs2276047 | 1.000 | 0.040 | 11 | 72230337 | intron variant | A/G | snv | 0.28 | 0.33 | 3 | |
| rs2292661 | 1.000 | 0.080 | 3 | 123150263 | missense variant | C/G;T | snv | 8.2E-04 | 3 | ||
| rs6978712 | 1.000 | 0.040 | 7 | 127507709 | intergenic variant | C/T | snv | 0.11 | 3 | ||
| rs7539020 | 1.000 | 0.040 | 1 | 230713444 | intron variant | C/T | snv | 0.43 | 3 | ||
| rs768349387 | 1.000 | 0.080 | 5 | 148827850 | missense variant | T/C | snv | 8.0E-06 | 3 | ||
| rs7690819 | 1.000 | 0.040 | 4 | 111199502 | intergenic variant | A/G;T | snv | 3 | |||
| rs7913948 | 1.000 | 0.080 | 10 | 45373441 | upstream gene variant | G/A | snv | 0.17 | 3 | ||
| rs920435389 | 1.000 | 0.040 | 5 | 177091064 | missense variant | G/C | snv | 3 | |||
| rs974453 | 1.000 | 0.080 | 12 | 20737008 | intron variant | A/G;T | snv | 3 | |||
| rs10489177 | 0.925 | 0.120 | 1 | 169793666 | missense variant | T/A;G | snv | 4.1E-06; 0.19 | 4 | ||
| rs1057293 | 0.925 | 0.120 | 6 | 134172259 | synonymous variant | G/A | snv | 0.12 | 0.11 | 4 | |
| rs1269801977 | 0.925 | 0.120 | 2 | 169604087 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 4 | |
| rs17118 | 0.925 | 0.120 | 3 | 38362981 | missense variant | C/A;T | snv | 0.29 | 4 | ||
| rs1873077 | 0.925 | 0.080 | 3 | 74273636 | intron variant | T/C | snv | 0.24 | 4 | ||
| rs3212335 | 1.000 | 0.080 | 15 | 26766994 | intron variant | C/T | snv | 0.32 | 4 | ||
| rs36217263 | 1.000 | 0.040 | 13 | 33015697 | upstream gene variant | A/- | del | 0.21 | 4 | ||
| rs7528153 | 0.925 | 0.080 | 1 | 107765105 | missense variant | T/A | snv | 0.58 | 0.64 | 4 | |
| rs768925824 | 0.925 | 0.040 | 19 | 11110693 | missense variant | G/A | snv | 4.0E-06 | 4 | ||
| rs891512 | 0.925 | 0.040 | 7 | 151011001 | intron variant | A/G | snv | 0.84 | 0.85 | 4 | |
| rs1037733674 | 0.882 | 0.120 | 2 | 162147429 | missense variant | T/C | snv | 1.4E-05 | 5 |