| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17133853 | 1.000 | 0.120 | 7 | 50501717 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
| rs4553808 | 0.672 | 0.320 | 2 | 203866282 | upstream gene variant | A/G;T | snv | 0.16 | 28 | ||
| rs4896310 | 1.000 | 0.120 | 6 | 138018697 | intergenic variant | A/G;T | snv | 3 | |||
| rs1110701 | 1.000 | 0.120 | 7 | 50410929 | intergenic variant | A/G;T | snv | 1 | |||
| rs2043211 | 0.653 | 0.480 | 19 | 48234449 | missense variant | A/T | snv | 0.33 | 0.29 | 29 | |
| rs6021191 | 0.851 | 0.120 | 20 | 51419700 | intron variant | A/T | snv | 4.9E-02 | 5 | ||
| rs34531324 | 1.000 | 0.120 | 5 | 174435441 | intron variant | A/T | snv | 0.16 | 3 | ||
| rs11770117 | 1.000 | 0.120 | 7 | 50406065 | downstream gene variant | A/T | snv | 0.41 | 2 | ||
| rs4947584 | 1.000 | 0.120 | 7 | 50505011 | intron variant | A/T | snv | 0.35 | 2 | ||
| rs1057519753 | 0.763 | 0.120 | 1 | 64846664 | missense variant | C/A | snv | 9 | |||
| rs10740055 | 0.790 | 0.240 | 10 | 61958720 | intron variant | C/A | snv | 0.49 | 7 | ||
| rs7088318 | 0.851 | 0.120 | 10 | 22564019 | intron variant | C/A | snv | 0.55 | 4 | ||
| rs147481775 | 1.000 | 0.120 | 22 | 31829377 | intron variant | C/A | snv | 6.6E-03 | 3 | ||
| rs11575575 | 1.000 | 0.120 | 7 | 50456510 | intron variant | C/A | snv | 7.5E-02 | 1 | ||
| rs121913451 | 0.851 | 0.160 | 9 | 130872903 | missense variant | C/A;G | snv | 4 | |||
| rs7818688 | 1.000 | 0.120 | 8 | 95011854 | intron variant | C/A;G | snv | 3 | |||
| rs7806674 | 1.000 | 0.120 | 7 | 50356265 | intron variant | C/A;G | snv | 1 | |||
| rs121913488 | 0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv | 7 | |||
| rs2274407 | 0.882 | 0.120 | 13 | 95206781 | missense variant | C/A;G;T | snv | 9.7E-02 | 0.10 | 4 | |
| rs10261922 | 1.000 | 0.120 | 7 | 50414314 | intergenic variant | C/A;G;T | snv | 1 | |||
| rs112141546 | 1.000 | 0.120 | 16 | 77367618 | missense variant | C/A;G;T | snv | 4.0E-06; 1.4E-03 | 1 | ||
| rs73195662 | 1.000 | 0.120 | 7 | 106018014 | missense variant | C/A;G;T | snv | 7.2E-02; 2.0E-05 | 1 | ||
| rs775144154 | 0.627 | 0.600 | 21 | 45531904 | missense variant | C/A;T | snv | 9.7E-06; 1.4E-05 | 38 |