| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1013210 | 1.000 | 0.040 | 8 | 24259209 | intergenic variant | G/A;C;T | snv | 1 | |||
| rs10280089 | 1.000 | 0.040 | 7 | 38667217 | intergenic variant | C/A;T | snv | 1 | |||
| rs11249215 | 1.000 | 0.040 | 1 | 24970693 | non coding transcript exon variant | G/A | snv | 0.44 | 1 | ||
| rs11578380 | 1.000 | 0.040 | 1 | 67295682 | intergenic variant | G/A;C | snv | 1 | |||
| rs11742270 | 1.000 | 0.040 | 5 | 35881341 | downstream gene variant | G/A | snv | 0.20 | 1 | ||
| rs12141575 | 1.000 | 0.040 | 1 | 67281753 | downstream gene variant | G/A | snv | 0.31 | 1 | ||
| rs13001372 | 1.000 | 0.040 | 2 | 62341086 | TF binding site variant | A/G | snv | 0.59 | 1 | ||
| rs13093489 | 1.000 | 0.040 | 3 | 27753416 | intergenic variant | C/A | snv | 0.35 | 1 | ||
| rs1383261 | 1.000 | 0.040 | 6 | 32797674 | regulatory region variant | C/T | snv | 0.38 | 1 | ||
| rs2242944 | 1.000 | 0.040 | 21 | 39093252 | intergenic variant | G/A | snv | 0.46 | 1 | ||
| rs2402752 | 1.000 | 0.040 | 7 | 124799545 | regulatory region variant | T/A;C | snv | 1 | |||
| rs2523522 | 1.000 | 0.040 | 6 | 31372551 | intron variant | T/A;C | snv | 1 | |||
| rs2531875 | 1.000 | 0.040 | 17 | 27821141 | intron variant | G/A;T | snv | 1 | |||
| rs30107 | 1.000 | 0.040 | 5 | 123756807 | regulatory region variant | A/G;T | snv | 1 | |||
| rs378108 | 1.000 | 0.040 | 21 | 39097594 | intergenic variant | A/G | snv | 0.42 | 1 | ||
| rs433130 | 1.000 | 0.040 | 4 | 166283823 | intergenic variant | G/A;C;T | snv | 1 | |||
| rs4648889 | 1.000 | 0.040 | 1 | 24967338 | upstream gene variant | G/A;T | snv | 1 | |||
| rs6502398 | 1.000 | 0.040 | 17 | 14832175 | upstream gene variant | A/C;T | snv | 1 | |||
| rs6759298 | 1.000 | 0.040 | 2 | 62341310 | regulatory region variant | G/A;C | snv | 1 | |||
| rs7743761 | 1.000 | 0.040 | 6 | 31368323 | intron variant | C/A | snv | 0.31 | 1 | ||
| rs8126528 | 1.000 | 0.040 | 21 | 39145849 | intergenic variant | A/G | snv | 0.89 | 1 | ||
| rs9379895 | 1.000 | 0.040 | 6 | 26592479 | upstream gene variant | A/G | snv | 0.19 | 1 | ||
| rs9468898 | 1.000 | 0.040 | 6 | 31214606 | intergenic variant | A/G | snv | 3.9E-02 | 1 | ||
| rs6979 | 1.000 | 0.040 | 16 | 67657765 | missense variant | A/G | snv | 0.50 | 0.61 | 1 | |
| rs14170 | 1.000 | 0.040 | 2 | 61188357 | synonymous variant | A/G;T | snv | 0.44; 4.0E-06 | 1 |