| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs762104961 | 0.882 | 0.200 | 17 | 46024014 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
| rs137853058 | 0.882 | 0.120 | 6 | 161973401 | missense variant | C/T | snv | 1.2E-05 | 3 | ||
| rs1801582 | 0.925 | 0.120 | 6 | 161386823 | missense variant | C/G;T | snv | 0.16; 3.2E-05 | 3 | ||
| rs201795631 | 0.882 | 0.200 | 9 | 132349336 | missense variant | T/C;G | snv | 8.0E-06; 8.0E-06 | 3 | ||
| rs1411478 | 0.925 | 0.120 | 1 | 180993146 | intron variant | A/G | snv | 0.56 | 3 | ||
| rs1038579230 | 0.882 | 0.200 | 9 | 35067913 | missense variant | C/A | snv | 3 | |||
| rs7571971 | 1.000 | 0.120 | 2 | 88595833 | non coding transcript exon variant | T/C | snv | 0.70 | 0.77 | 2 | |
| rs11568563 | 0.925 | 0.240 | 12 | 21304500 | missense variant | T/G | snv | 4.5E-02 | 4.4E-02 | 2 | |
| rs114573015 | 1.000 | 0.120 | 1 | 85137368 | downstream gene variant | A/G | snv | 1.1E-02 | 1 | ||
| rs12125383 | 1.000 | 0.120 | 1 | 221995092 | regulatory region variant | G/A | snv | 0.14 | 1 | ||
| rs2142991 | 1.000 | 0.120 | 10 | 42845657 | intergenic variant | C/G;T | snv | 1 | |||
| rs6852535 | 1.000 | 0.120 | 4 | 122557561 | intergenic variant | G/A | snv | 0.24 | 1 | ||
| rs2045091 | 1.000 | 0.120 | 8 | 130063613 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs368453549 | 1.000 | 0.120 | 19 | 15272936 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs566433112 | 1.000 | 0.120 | 2 | 74378112 | missense variant | T/C | snv | 1.6E-05 | 2.1E-05 | 1 | |
| rs76970862 | 1.000 | 0.120 | 17 | 45709317 | intron variant | A/G | snv | 4.6E-02 | 1 | ||
| rs1425322249 | 1.000 | 0.120 | 5 | 96979369 | missense variant | G/A | snv | 1 | |||
| rs6547705 | 1.000 | 0.120 | 2 | 86817193 | intron variant | G/A | snv | 0.83 | 1 | ||
| rs10878245 | 1.000 | 0.120 | 12 | 40237989 | missense variant | T/A;C | snv | 0.52 | 1 | ||
| rs10675541 | 1.000 | 0.120 | 3 | 39468795 | intron variant | -/CA | delins | 1 | |||
| rs621042 | 1.000 | 0.120 | 12 | 18636073 | intron variant | C/A | snv | 0.36 | 1 | ||
| rs35740963 | 1.000 | 0.120 | 6 | 45531876 | intron variant | -/T | delins | 1 | |||
| rs7966334 | 1.000 | 0.120 | 12 | 21314281 | intron variant | C/G | snv | 0.95 | 1 | ||
| rs746389377 | 1.000 | 0.120 | 10 | 95384258 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs147124286 | 1.000 | 0.120 | 12 | 53394218 | intron variant | -/A | delins | 0.18 | 1 |