| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2280141 | 1.000 | 0.040 | 10 | 122433665 | 3 prime UTR variant | T/G | snv | 0.56 | 4 | ||
| rs10892279 | 1.000 | 0.120 | 11 | 118741072 | intron variant | G/A;T | snv | 0.25 | 3 | ||
| rs1228534100 | 1.000 | 0.040 | 12 | 120978892 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
| rs13031237 | 1.000 | 0.120 | 2 | 60908994 | intron variant | G/T | snv | 0.25 | 3 | ||
| rs1953126 | 1.000 | 0.120 | 9 | 120878222 | intron variant | T/C | snv | 0.68 | 3 | ||
| rs212402 | 1.000 | 0.080 | 6 | 159051263 | intron variant | G/A | snv | 0.66 | 3 | ||
| rs2249937 | 1.000 | 0.080 | 6 | 159094277 | non coding transcript exon variant | T/G | snv | 0.76 | 3 | ||
| rs4648356 | 1.000 | 0.080 | 1 | 2792599 | intron variant | C/A | snv | 0.39 | 3 | ||
| rs654690 | 1.000 | 0.080 | 6 | 159093746 | intron variant | T/A;C | snv | 3 | |||
| rs6585827 | 1.000 | 0.040 | 10 | 122406099 | intron variant | G/A | snv | 0.47 | 3 | ||
| rs6726160 | 1.000 | 0.080 | 2 | 60937594 | non coding transcript exon variant | T/G | snv | 0.47 | 3 | ||
| rs6848139 | 1.000 | 0.040 | 4 | 122473886 | intergenic variant | A/C;G | snv | 3 | |||
| rs715412 | 1.000 | 0.080 | 11 | 118813901 | regulatory region variant | G/A | snv | 0.17 | 3 | ||
| rs7523907 | 1.000 | 0.080 | 1 | 167458010 | non coding transcript exon variant | C/A;T | snv | 3 | |||
| rs7573065 | 1.000 | 0.120 | 2 | 218381984 | upstream gene variant | C/A;T | snv | 3 | |||
| rs76857106 | 1.000 | 0.120 | 19 | 12806782 | missense variant | G/A | snv | 3 | |||
| rs11204735 | 1.000 | 0.080 | 1 | 150869191 | intron variant | T/C | snv | 0.41 | 2 | ||
| rs11711054 | 1.000 | 0.080 | 3 | 46304120 | intergenic variant | G/A | snv | 0.73 | 2 | ||
| rs12115114 | 1.000 | 0.080 | 8 | 63477322 | non coding transcript exon variant | A/G;T | snv | 2 | |||
| rs1223438908 | 1.000 | 0.120 | 3 | 105681480 | missense variant | T/G | snv | 4.0E-06 | 2 | ||
| rs1252641479 | 1.000 | 0.040 | 13 | 111300800 | missense variant | T/G | snv | 4.0E-06 | 2 | ||
| rs12992492 | 1.000 | 0.040 | 2 | 203836831 | intergenic variant | A/G | snv | 0.40 | 2 | ||
| rs140101069 | 1.000 | 0.120 | 9 | 3828342 | missense variant | G/A | snv | 3.2E-04 | 8.4E-05 | 2 | |
| rs140490 | 1.000 | 0.080 | 22 | 21567397 | intron variant | G/A;C;T | snv | 2 | |||
| rs1425186769 | 1.000 | 0.120 | 12 | 132620303 | missense variant | C/T | snv | 4.4E-05 | 3.5E-05 | 2 |