| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11073058 | 1.000 | 0.040 | 15 | 34697425 | regulatory region variant | G/A;T | snv | 3 | |||
| rs4074961 | 1.000 | 0.040 | 1 | 37627051 | intron variant | C/T | snv | 0.39 | 3 | ||
| rs1107946 | 1.000 | 0.040 | 17 | 50203629 | intron variant | A/C | snv | 0.80 | 2 | ||
| rs12321 | 1.000 | 0.040 | 22 | 29057205 | 3 prime UTR variant | G/C | snv | 0.38 | 2 | ||
| rs9811920 | 1.000 | 0.040 | 3 | 100125449 | intron variant | G/A | snv | 0.43 | 2 | ||
| rs994767 | 1.000 | 0.040 | 1 | 219602090 | intergenic variant | A/G | snv | 0.56 | 2 | ||
| rs1003483 | 1.000 | 0.040 | 11 | 2146313 | non coding transcript exon variant | T/G | snv | 0.47 | 0.40 | 1 | |
| rs10215153 | 1.000 | 0.040 | 7 | 116759077 | intron variant | G/A | snv | 0.32 | 1 | ||
| rs116126526 | 1.000 | 0.040 | 1 | 203503710 | missense variant | G/A | snv | 1.2E-03 | 2.6E-03 | 1 | |
| rs11746675 | 1.000 | 0.040 | 5 | 178986946 | synonymous variant | T/C | snv | 0.60 | 0.57 | 1 | |
| rs12421026 | 1.000 | 0.040 | 11 | 31787774 | 3 prime UTR variant | C/G;T | snv | 1 | |||
| rs146113475 | 1.000 | 0.040 | 6 | 47286087 | missense variant | G/A | snv | 1.6E-05 | 3.5E-05 | 1 | |
| rs1516794 | 1.000 | 0.040 | 15 | 88861672 | intron variant | A/T | snv | 5.3E-03 | 1 | ||
| rs1886970 | 1.000 | 0.040 | 13 | 23866359 | intron variant | T/C | snv | 0.39 | 1 | ||
| rs2067011 | 1.000 | 0.040 | 5 | 178988936 | splice region variant | A/G | snv | 0.53 | 0.51 | 1 | |
| rs2229336 | 1.000 | 0.040 | 18 | 3457778 | synonymous variant | T/G | snv | 1.9E-02 | 5.5E-02 | 1 | |
| rs2229429 | 1.000 | 0.040 | 19 | 7166377 | missense variant | G/A;C;T | snv | 0.20; 1.6E-05 | 1 | ||
| rs2236475 | 1.000 | 0.040 | 21 | 45495128 | 3 prime UTR variant | A/G | snv | 0.32 | 1 | ||
| rs2269336 | 1.000 | 0.040 | 17 | 50202995 | intron variant | G/A;C | snv | 1 | |||
| rs2645339 | 1.000 | 0.040 | 5 | 178989062 | synonymous variant | G/A | snv | 0.53 | 0.50 | 1 | |
| rs28730814 | 1.000 | 0.040 | 16 | 55496952 | missense variant | G/A;C;T | snv | 1.3E-03; 1.1E-04; 4.0E-06 | 1 | ||
| rs3026390 | 1.000 | 0.040 | 11 | 31791961 | non coding transcript exon variant | T/A;C | snv | 0.44 | 1 | ||
| rs35766 | 1.000 | 0.040 | 12 | 102486695 | upstream gene variant | C/T | snv | 0.71 | 1 | ||
| rs368943069 | 1.000 | 0.040 | 4 | 121678449 | missense variant | C/T | snv | 1 | |||
| rs3745551 | 1.000 | 0.040 | 19 | 7114277 | 3 prime UTR variant | C/T | snv | 0.67 | 1 |