| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4712656 | 1.000 | 0.040 | 6 | 22136033 | non coding transcript exon variant | G/A;C | snv | 4 | |||
| 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 | |||
| rs10131293 | 1.000 | 0.040 | 14 | 22461166 | intron variant | G/A | snv | 0.15 | 1 | ||
| rs10132733 | 1.000 | 0.040 | 14 | 22477241 | intron variant | A/G | snv | 0.19 | 1 | ||
| rs10142552 | 1.000 | 0.040 | 14 | 22395232 | intron variant | G/A | snv | 3.5E-02 | 1 | ||
| rs10148895 | 1.000 | 0.040 | 14 | 22254840 | intron variant | C/T | snv | 0.18 | 1 | ||
| rs10155916 | 1.000 | 0.040 | 7 | 38286177 | intergenic variant | G/A | snv | 0.11 | 1 | ||
| rs10162417 | 1.000 | 0.040 | 14 | 22460708 | intron variant | T/G | snv | 0.15 | 1 | ||
| rs1040303 | 1.000 | 0.040 | 14 | 22403377 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs10441090 | 1.000 | 0.040 | 7 | 38295217 | upstream gene variant | C/T | snv | 0.13 | 1 | ||
| rs10483273 | 1.000 | 0.040 | 14 | 22448054 | intron variant | A/G | snv | 9.5E-02 | 1 | ||
| rs10483275 | 1.000 | 0.040 | 14 | 22464064 | intron variant | C/T | snv | 9.5E-02 | 1 | ||
| rs10483277 | 1.000 | 0.040 | 14 | 22471852 | intron variant | C/G;T | snv | 1 | |||
| rs10487742 | 1.000 | 0.040 | 7 | 38326911 | non coding transcript exon variant | G/A | snv | 0.14 | 1 | ||
| rs10742682 | 1.000 | 0.040 | 11 | 43644307 | non coding transcript exon variant | C/T | snv | 0.38 | 1 | ||
| rs1076861 | 1.000 | 0.040 | 14 | 22473629 | intron variant | G/A | snv | 0.10 | 1 | ||
| rs10932572 | 1.000 | 0.040 | 2 | 214762673 | intron variant | A/G | snv | 0.42 | 1 | ||
| rs11157596 | 1.000 | 0.040 | 14 | 22438076 | intron variant | G/A | snv | 0.58 | 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 | ||
| rs11623995 | 1.000 | 0.040 | 14 | 22436733 | intron variant | A/G | snv | 0.74 | 1 | ||
| rs11624054 | 1.000 | 0.040 | 14 | 22406085 | intron variant | A/G | snv | 0.71 | 1 | ||
| rs11765884 | 1.000 | 0.040 | 7 | 38317722 | 5 prime UTR variant | C/T | snv | 0.20 | 1 | ||
| rs11769443 | 1.000 | 0.040 | 7 | 38317474 | missense variant | T/C | snv | 0.39 | 0.42 | 1 |