| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10034228 | 0.882 | 0.040 | 4 | 111690594 | intergenic variant | T/C | snv | 0.32 | 3 | ||
| rs1003483 | 1.000 | 0.040 | 11 | 2146313 | non coding transcript exon variant | T/G | snv | 0.47 | 0.40 | 1 | |
| rs10046 | 0.708 | 0.400 | 15 | 51210789 | 3 prime UTR variant | G/A | snv | 0.45 | 0.43 | 18 | |
| rs10215153 | 1.000 | 0.040 | 7 | 116759077 | intron variant | G/A | snv | 0.32 | 1 | ||
| rs1057518802 | 0.882 | 0.080 | 21 | 45509554 | stop gained | C/T | snv | 4 | |||
| rs1057518836 | 0.882 | 0.120 | X | 43949887 | missense variant | G/A | snv | 4 | |||
| rs1057524237 | 0.851 | 0.280 | 1 | 102915626 | splice region variant | C/T | snv | 7 | |||
| rs10824518 | 0.882 | 0.040 | 10 | 77303784 | intron variant | T/A;C | snv | 3 | |||
| rs10860860 | 0.925 | 0.040 | 12 | 102387055 | non coding transcript exon variant | A/T | snv | 0.28 | 2 | ||
| rs11073058 | 1.000 | 0.040 | 15 | 34697425 | regulatory region variant | G/A;T | snv | 3 | |||
| rs1107946 | 1.000 | 0.040 | 17 | 50203629 | intron variant | A/C | snv | 0.80 | 2 | ||
| 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 | |
| rs121918327 | 0.776 | 0.240 | 4 | 122742955 | stop gained | C/T | snv | 2.8E-05 | 1.4E-05 | 12 | |
| rs12321 | 1.000 | 0.040 | 22 | 29057205 | 3 prime UTR variant | G/C | snv | 0.38 | 2 | ||
| rs12421026 | 1.000 | 0.040 | 11 | 31787774 | 3 prime UTR variant | C/G;T | snv | 1 | |||
| rs12423791 | 0.925 | 0.040 | 12 | 102465050 | intron variant | G/C | snv | 2.8E-02 | 5 | ||
| rs12716080 | 0.882 | 0.040 | 5 | 11166836 | intron variant | G/T | snv | 0.39 | 3 | ||
| rs13095226 | 0.851 | 0.040 | 3 | 99677428 | intron variant | T/C | snv | 9.5E-02 | 5 | ||
| rs13382811 | 0.882 | 0.040 | 2 | 144466053 | intron variant | C/T | snv | 0.21 | 4 | ||
| rs137854466 | 0.724 | 0.320 | 15 | 48411280 | stop gained | G/A;C | snv | 4.0E-05; 8.0E-06 | 23 | ||
| rs1425998598 | 0.763 | 0.240 | 17 | 67918802 | missense variant | G/A;C | snv | 1.2E-05 | 19 | ||
| 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 | ||
| rs1554121443 | 0.742 | 0.280 | 6 | 33438873 | stop gained | C/T | snv | 29 |