| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1332018 | 0.882 | 0.200 | 1 | 109740350 | 5 prime UTR variant | G/T | snv | 0.64 | 0.66 | 6 | |
| rs140501902 | 0.807 | 0.160 | 1 | 226883774 | missense variant | C/T | snv | 3.6E-03 | 3.4E-03 | 6 | |
| rs3818361 | 0.851 | 0.080 | 1 | 207611623 | intron variant | A/G | snv | 0.74 | 6 | ||
| rs80356715 | 0.807 | 0.120 | 1 | 11016874 | missense variant | C/G;T | snv | 8.0E-06; 2.2E-04 | 6 | ||
| rs1977412 | 0.882 | 0.160 | 1 | 230716523 | intron variant | T/A;C | snv | 5 | |||
| rs213045 | 0.851 | 0.120 | 1 | 21290752 | intron variant | G/T | snv | 0.44 | 5 | ||
| rs28936380 | 0.827 | 0.080 | 1 | 226885546 | missense variant | C/G;T | snv | 1.2E-05 | 5 | ||
| rs533813519 | 0.851 | 0.120 | 1 | 226888097 | missense variant | C/A | snv | 1.9E-04 | 4.2E-05 | 5 | |
| rs6336 | 0.827 | 0.120 | 1 | 156879126 | missense variant | C/T | snv | 4.2E-02 | 3.7E-02 | 5 | |
| rs63749884 | 0.851 | 0.160 | 1 | 226888979 | missense variant | G/A | snv | 5 | |||
| rs678849 | 0.882 | 0.120 | 1 | 28818676 | intron variant | C/T | snv | 0.44 | 5 | ||
| rs12752888 | 0.851 | 0.160 | 1 | 54527266 | downstream gene variant | T/C | snv | 0.26 | 4 | ||
| rs17646665 | 1.000 | 0.080 | 1 | 109369429 | intron variant | A/G | snv | 5.8E-02 | 4 | ||
| rs61812598 | 1.000 | 0.080 | 1 | 154447611 | intron variant | G/A | snv | 0.31 | 4 | ||
| rs890293 | 0.851 | 0.200 | 1 | 59926822 | upstream gene variant | C/A | snv | 8.6E-02 | 4 | ||
| rs58973334 | 0.882 | 0.080 | 1 | 226883748 | missense variant | G/A | snv | 8.6E-03 | 1.4E-02 | 3 | |
| rs61761208 | 0.882 | 0.080 | 1 | 226885602 | missense variant | A/T | snv | 3 | |||
| rs6334 | 1.000 | 0.080 | 1 | 156876441 | missense variant | G/A;C;T | snv | 0.22; 4.0E-06 | 3 | ||
| rs823118 | 0.925 | 0.080 | 1 | 205754444 | upstream gene variant | C/A;T | snv | 3 | |||
| rs1344800847 | 0.925 | 0.120 | 1 | 207569911 | missense variant | G/T | snv | 2 | |||
| rs200169735 | 0.925 | 0.080 | 1 | 226895498 | missense variant | C/G;T | snv | 4.0E-06; 2.8E-05 | 2 | ||
| rs2296160 | 0.925 | 0.120 | 1 | 207621975 | missense variant | A/G | snv | 0.82 | 0.81 | 2 | |
| rs3738467 | 0.925 | 0.120 | 1 | 207552816 | missense variant | G/T | snv | 1.4E-03 | 2 | ||
| rs4575098 | 1.000 | 0.080 | 1 | 161185602 | 3 prime UTR variant | G/A | snv | 0.18 | 2 | ||
| rs600491 | 0.925 | 0.080 | 1 | 54867852 | intron variant | C/A;T | snv | 2 |