| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2048417 | 1.000 | 0.080 | 3 | 191064734 | intergenic variant | C/T | snv | 0.53 | 1 | ||
| rs2168708 | 1.000 | 0.080 | 18 | 60240078 | intergenic variant | G/T | snv | 0.20 | 1 | ||
| rs2185937 | 1.000 | 0.080 | 10 | 117945191 | intergenic variant | C/G | snv | 0.46 | 1 | ||
| rs259067 | 1.000 | 0.080 | 5 | 79803175 | intron variant | C/T | snv | 0.22 | 1 | ||
| rs2784243 | 1.000 | 0.080 | 6 | 51589842 | intergenic variant | C/T | snv | 0.66 | 1 | ||
| rs41492957 | 1.000 | 0.080 | 20 | 16988369 | intergenic variant | C/T | snv | 0.13 | 1 | ||
| rs4285184 | 1.000 | 0.080 | 5 | 180779656 | intergenic variant | A/G | snv | 0.41 | 1 | ||
| rs4615388 | 1.000 | 0.080 | 6 | 51282222 | intergenic variant | T/A | snv | 0.22 | 1 | ||
| rs477181 | 1.000 | 0.080 | 18 | 60228805 | intergenic variant | G/A;T | snv | 1 | |||
| rs492443 | 1.000 | 0.080 | 18 | 60191569 | upstream gene variant | A/G | snv | 0.32 | 1 | ||
| rs502933 | 1.000 | 0.080 | 18 | 60229241 | intergenic variant | C/A | snv | 0.38 | 1 | ||
| rs516175 | 1.000 | 0.080 | 8 | 9912063 | intergenic variant | G/A | snv | 0.15 | 1 | ||
| rs590215 | 1.000 | 0.080 | 18 | 60236855 | intergenic variant | C/T | snv | 0.23 | 1 | ||
| rs734597 | 1.000 | 0.080 | 6 | 50868566 | intergenic variant | G/A | snv | 0.16 | 1 | ||
| rs7379701 | 1.000 | 0.080 | 5 | 71715685 | upstream gene variant | T/C;G | snv | 1 | |||
| rs7474896 | 1.000 | 0.080 | 10 | 37693169 | intergenic variant | C/T | snv | 0.11 | 1 | ||
| rs7520850 | 1.000 | 0.080 | 1 | 46417996 | downstream gene variant | G/A;C | snv | 1 | |||
| rs7581710 | 1.000 | 0.080 | 2 | 120437605 | regulatory region variant | A/G | snv | 0.16 | 1 | ||
| rs7655505 | 1.000 | 0.080 | 4 | 32296333 | intergenic variant | C/T | snv | 0.42 | 1 | ||
| rs7826222 | 1.000 | 0.080 | 8 | 10002570 | intron variant | G/C | snv | 1 | |||
| rs8083289 | 1.000 | 0.080 | 18 | 60226385 | intergenic variant | C/A;G | snv | 1 | |||
| rs9568856 | 1.000 | 0.080 | 13 | 53490846 | intron variant | G/A;C | snv | 1 | |||
| rs9892622 | 1.000 | 0.080 | 17 | 78350041 | downstream gene variant | G/A | snv | 0.50 | 1 | ||
| rs9947301 | 1.000 | 0.080 | 18 | 60202357 | downstream gene variant | C/T | snv | 9.7E-02 | 1 | ||
| rs9956279 | 1.000 | 0.080 | 18 | 60275566 | intergenic variant | C/A;T | snv | 1 |