| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 | ||
| rs12826786 | 0.683 | 0.480 | 12 | 53961717 | upstream gene variant | C/T | snv | 0.38 | 26 | ||
| rs874945 | 0.732 | 0.240 | 12 | 53961667 | upstream gene variant | C/T | snv | 0.38 | 14 | ||
| rs7652589 | 0.732 | 0.400 | 3 | 122170241 | downstream gene variant | A/G | snv | 0.60 | 13 | ||
| rs11994014 | 0.827 | 0.200 | 8 | 24944767 | intergenic variant | A/G | snv | 0.70 | 5 | ||
| rs11103603 | 0.851 | 0.080 | 9 | 134449754 | TF binding site variant | T/C | snv | 0.46 | 4 | ||
| rs1027702 | 0.882 | 0.080 | 1 | 161743067 | intergenic variant | C/T | snv | 0.51 | 3 | ||
| rs10840002 | 0.882 | 0.080 | 11 | 8221479 | downstream gene variant | A/G | snv | 0.49 | 3 | ||
| rs12442054 | 0.882 | 0.080 | 15 | 74165683 | intron variant | G/A | snv | 0.12 | 3 | ||
| rs4758051 | 0.882 | 0.080 | 11 | 8217092 | intergenic variant | G/A | snv | 0.42 | 3 | ||
| rs2367486 | 1.000 | 0.040 | 7 | 142784320 | upstream gene variant | A/G | snv | 0.50 | 2 | ||
| rs6959895 | 1.000 | 0.040 | 7 | 142727107 | non coding transcript exon variant | T/A;C | snv | 2 | |||
| rs10148895 | 1.000 | 0.040 | 14 | 22254840 | intron variant | C/T | snv | 0.18 | 1 | ||
| rs10441090 | 1.000 | 0.040 | 7 | 38295217 | upstream gene variant | C/T | snv | 0.13 | 1 | ||
| rs10487742 | 1.000 | 0.040 | 7 | 38326911 | non coding transcript exon variant | G/A | snv | 0.14 | 1 | ||
| rs11579261 | 1.000 | 0.040 | 1 | 143544453 | intron variant | T/A;C | snv | 1 | |||
| rs11587304 | 1.000 | 0.040 | 1 | 143653074 | upstream gene variant | A/C | snv | 0.83 | 1 | ||
| rs11975431 | 1.000 | 0.040 | 7 | 38322024 | upstream gene variant | C/T | snv | 0.14 | 1 | ||
| rs11984094 | 1.000 | 0.040 | 7 | 38323965 | upstream gene variant | A/G | snv | 0.14 | 1 | ||
| rs12154478 | 1.000 | 0.040 | 7 | 38290217 | downstream gene variant | G/A | snv | 6.9E-02 | 1 | ||
| rs12881142 | 1.000 | 0.040 | 14 | 22268637 | intron variant | C/A;T | snv | 1 | |||
| rs12888049 | 1.000 | 0.040 | 14 | 22026498 | regulatory region variant | G/A | snv | 0.30 | 1 | ||
| rs17113407 | 1.000 | 0.040 | 14 | 22020341 | intergenic variant | T/C | snv | 6.7E-02 | 1 | ||
| rs17161949 | 1.000 | 0.040 | 1 | 143550435 | intron variant | T/C | snv | 6.4E-02 | 1 | ||
| rs17162082 | 1.000 | 0.040 | 1 | 143545399 | intron variant | C/T | snv | 5.0E-02 | 1 |