| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs80356711 | 1.000 | 20 | 4699698 | stop gained | C/T | snv | 4 | ||||
| rs10509125 | 10 | 60167108 | intron variant | C/A | snv | 0.56 | 2 | ||||
| rs1016726 | 7 | 29316787 | intron variant | G/A | snv | 0.12 | 1 | ||||
| rs1188539174 | 12 | 40232341 | missense variant | C/T | snv | 4.0E-06 | 1 | ||||
| rs1292160648 | 20 | 4699738 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 1 | |||
| rs2756271 | 20 | 4684616 | intron variant | A/G;T | snv | 1 | |||||
| rs6052751 | 20 | 4664427 | intron variant | G/A;C | snv | 1 | |||||
| rs6116477 | 20 | 4704015 | downstream gene variant | T/C | snv | 0.23 | 1 | ||||
| rs747500244 | 20 | 4699797 | missense variant | A/G | snv | 1.2E-05 | 1 | ||||
| rs768562045 | 20 | 4699821 | missense variant | A/T | snv | 4.0E-06 | 1 | ||||
| rs775144659 | 20 | 4699816 | missense variant | C/A | snv | 1 | |||||
| rs12817488 | 1.000 | 0.040 | 12 | 122811747 | intron variant | G/A | snv | 0.39 | 3 | ||
| rs80356710 | 0.925 | 0.040 | 20 | 4699655 | stop gained | T/G | snv | 3 | |||
| rs947211 | 0.925 | 0.040 | 1 | 205783537 | non coding transcript exon variant | A/G | snv | 0.64 | 3 | ||
| rs10994443 | 1.000 | 0.040 | 10 | 60635760 | intron variant | G/A | snv | 0.11 | 2 | ||
| rs1994090 | 1.000 | 0.040 | 12 | 40034759 | intron variant | G/A;T | snv | 2 | |||
| rs4538475 | 1.000 | 0.040 | 4 | 15736314 | intron variant | A/G | snv | 0.24 | 2 | ||
| rs610932 | 0.851 | 0.080 | 11 | 60171834 | downstream gene variant | T/G | snv | 0.57 | 5 | ||
| rs11767557 | 0.882 | 0.080 | 7 | 143412046 | intron variant | T/C | snv | 0.18 | 4 | ||
| rs2736990 | 0.882 | 0.080 | 4 | 89757390 | intron variant | G/A;T | snv | 4 | |||
| rs597668 | 0.925 | 0.080 | 19 | 45205630 | intron variant | T/A;C;G | snv | 3 | |||
| rs670139 | 0.925 | 0.080 | 11 | 60204322 | intron variant | G/A;T | snv | 3 | |||
| rs12734001 | 1.000 | 0.080 | 1 | 202421786 | intron variant | C/T | snv | 3.5E-05 | 2 | ||
| rs267606980 | 1.000 | 0.080 | 20 | 4699600 | missense variant | G/T | snv | 4.0E-06 | 2 | ||
| rs9349407 | 1.000 | 0.080 | 6 | 47485642 | intron variant | G/C | snv | 0.23 | 2 |