| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1145612 | 1.000 | 0.120 | 5 | 158271107 | upstream gene variant | C/A | snv | 0.49 | 1 | ||
| rs114790220 | 1.000 | 0.120 | 8 | 5306434 | intergenic variant | T/A;C | snv | 1 | |||
| rs11662496 | 1.000 | 0.120 | 18 | 43695432 | intergenic variant | A/G;T | snv | 1 | |||
| rs11771617 | 1.000 | 0.120 | 7 | 125733372 | intergenic variant | A/G | snv | 0.20 | 1 | ||
| rs13064954 | 1.000 | 0.120 | 3 | 157136953 | downstream gene variant | G/A | snv | 7.9E-02 | 1 | ||
| rs17404956 | 1.000 | 0.120 | 5 | 166962488 | regulatory region variant | A/G | snv | 5.5E-02 | 1 | ||
| rs2104455 | 1.000 | 0.120 | 6 | 9368285 | intergenic variant | A/G | snv | 0.30 | 1 | ||
| rs227453 | 1.000 | 0.120 | 6 | 165065309 | intron variant | A/T | snv | 0.18 | 1 | ||
| rs227455 | 1.000 | 0.120 | 6 | 165064562 | intron variant | T/C | snv | 0.17 | 1 | ||
| rs3007729 | 1.000 | 0.120 | 1 | 18468761 | regulatory region variant | T/C;G | snv | 1 | |||
| rs4470583 | 1.000 | 0.120 | 4 | 161329780 | intergenic variant | A/G;T | snv | 1 | |||
| rs74152685 | 1.000 | 0.120 | 1 | 247647989 | intron variant | G/T | snv | 4.4E-02 | 1 | ||
| rs200903070 | 1.000 | 0.120 | 7 | 134448044 | missense variant | G/A | snv | 6.4E-05 | 1.1E-04 | 1 | |
| rs140421861 | 1.000 | 0.120 | 4 | 73413512 | synonymous variant | C/T | snv | 1.1E-04 | 1.1E-04 | 1 | |
| rs10491034 | 1.000 | 0.120 | 10 | 48602322 | intron variant | G/A;T | snv | 1 | |||
| rs3844492 | 1.000 | 0.120 | 10 | 48614756 | intron variant | A/G | snv | 0.38 | 1 | ||
| rs11567245 | 1.000 | 0.120 | 7 | 82151406 | intron variant | T/A | snv | 1 | |||
| rs39059 | 1.000 | 0.120 | 7 | 29215854 | intron variant | A/G | snv | 0.32 | 1 | ||
| rs139876191 | 1.000 | 0.120 | 6 | 34242693 | intron variant | -/C | delins | 7.7E-02; 5.8E-06 | 5.2E-02 | 1 | |
| rs2038823 | 1.000 | 0.120 | 13 | 96299179 | intron variant | G/A;T | snv | 1 | |||
| rs954226380 | 1.000 | 0.120 | 12 | 49054970 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs148995025 | 1.000 | 0.120 | 5 | 7085094 | intron variant | A/G | snv | 8.9E-03 | 1 | ||
| rs1711347 | 1.000 | 0.120 | 1 | 243998680 | intron variant | G/A | snv | 0.53 | 1 | ||
| rs476141 | 1.000 | 0.120 | 1 | 244013122 | intron variant | G/A;T | snv | 1 | |||
| rs512825 | 1.000 | 0.120 | 1 | 244006892 | intron variant | A/G | snv | 0.39 | 1 |