| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1880243 | 1.000 | 0.040 | 7 | 22720036 | intron variant | C/A | snv | 0.18 | 1 | ||
| rs199472856 | 1.000 | 0.040 | 7 | 150974717 | stop gained | T/A;C | snv | 1 | |||
| rs199473627 | 1.000 | 0.040 | 3 | 38551258 | missense variant | A/G | snv | 1 | |||
| rs2267734 | 1.000 | 0.040 | 7 | 31095857 | intron variant | G/A | snv | 0.56 | 1 | ||
| rs2302475 | 1.000 | 0.040 | 7 | 31081886 | intron variant | T/C | snv | 0.48 | 1 | ||
| rs3906956 | 1.000 | 0.040 | 18 | 26856350 | missense variant | A/G | snv | 1 | |||
| rs72878794 | 1.000 | 0.040 | 18 | 26866839 | intron variant | C/A;T | snv | 8.1E-02 | 1 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs751377893 | 0.574 | 0.680 | 1 | 169546513 | missense variant | T/C | snv | 4.0E-06 | 65 | ||
| rs72546668 | 0.807 | 0.200 | 3 | 8745644 | missense variant | C/A;T | snv | 4.0E-06; 2.6E-03 | 8 | ||
| rs1310230286 | 1.000 | 0.040 | 3 | 38604872 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 15 | ||
| rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 49 | ||
| rs1188884950 | 0.925 | 0.080 | 5 | 474952 | missense variant | A/G | snv | 4.2E-06 | 2 | ||
| rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
| rs199473124 | 0.851 | 0.120 | 3 | 38603902 | missense variant | A/T | snv | 8.0E-06 | 7.0E-06 | 4 | |
| rs199473097 | 0.763 | 0.120 | 3 | 38606710 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 9 | |
| rs1801030 | 1.000 | 0.040 | 16 | 28606164 | missense variant | C/G;T | snv | 8.1E-06; 0.98 | 1 | ||
| rs199473190 | 1.000 | 0.040 | 3 | 38579474 | missense variant | C/G;T | snv | 8.2E-06 | 1 | ||
| rs1805123 | 0.724 | 0.280 | 7 | 150948446 | missense variant | T/A;C;G | snv | 1.3E-05; 0.18; 8.4E-06 | 18 | ||
| rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
| rs368660364 | 1.000 | 0.040 | 20 | 33408748 | missense variant | C/T | snv | 1.6E-05 | 2.8E-05 | 1 | |
| rs199473573 | 0.925 | 0.120 | 3 | 38604007 | missense variant | A/C | snv | 1.6E-05 | 7.0E-06 | 2 | |
| rs7626962 | 0.790 | 0.080 | 3 | 38579416 | missense variant | G/A;T | snv | 1.6E-05; 5.9E-03 | 10 | ||
| rs137854610 | 0.925 | 0.120 | 3 | 38550895 | missense variant | C/T | snv | 2.8E-05 | 1.7E-04 | 2 |