| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61907710 | 1.000 | 0.040 | 11 | 128287970 | intergenic variant | C/A;T | snv | 1 | |||
| rs61938962 | 1.000 | 0.040 | 12 | 56052982 | intergenic variant | C/T | snv | 0.26 | 1 | ||
| rs62172472 | 1.000 | 0.040 | 2 | 187163590 | intron variant | G/A;T | snv | 1 | |||
| rs6986151 | 1.000 | 0.040 | 8 | 100507673 | downstream gene variant | T/C | snv | 0.20 | 1 | ||
| rs709498 | 1.000 | 0.040 | 3 | 107975987 | regulatory region variant | A/G;T | snv | 1 | |||
| rs75084216 | 1.000 | 0.040 | 1 | 172670579 | downstream gene variant | C/T | snv | 2.7E-02 | 1 | ||
| rs9300546 | 1.000 | 0.040 | 13 | 99435465 | upstream gene variant | T/A;G | snv | 1 | |||
| rs940341 | 1.000 | 0.040 | 2 | 227860010 | intergenic variant | A/C;G | snv | 1 | |||
| rs981625 | 1.000 | 0.040 | 13 | 73465798 | intron variant | C/G | snv | 4.4E-02 | 1 | ||
| rs71373536 | 1.000 | 0.040 | 17 | 45144441 | upstream gene variant | G/A | snv | 0.19 | 1 | ||
| rs1904522 | 1.000 | 0.040 | 4 | 122415763 | intron variant | G/A | snv | 0.29 | 1 | ||
| rs2746438 | 1.000 | 0.040 | 6 | 135396930 | intron variant | T/A | snv | 0.68 | 1 | ||
| rs1448190 | 1.000 | 0.040 | 2 | 111618386 | intron variant | A/C | snv | 0.68 | 1 | ||
| rs61832952 | 1.000 | 0.040 | 10 | 5885488 | intron variant | T/C | snv | 0.11 | 1 | ||
| rs16858573 | 1.000 | 0.040 | 2 | 143118156 | intron variant | T/C | snv | 8.7E-02 | 1 | ||
| rs905670 | 1.000 | 0.040 | 6 | 90248783 | intron variant | G/A | snv | 0.25 | 1 | ||
| rs12068304 | 1.000 | 0.040 | 1 | 212691650 | intron variant | A/G | snv | 0.20 | 1 | ||
| rs10756796 | 1.000 | 0.040 | 9 | 16730976 | intron variant | A/G | snv | 0.43 | 1 | ||
| rs8068844 | 1.000 | 0.040 | 17 | 42419266 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs11783015 | 1.000 | 0.040 | 8 | 128682763 | intron variant | T/C | snv | 0.23 | 1 | ||
| rs61886887 | 1.000 | 0.040 | 11 | 64352979 | non coding transcript exon variant | C/T | snv | 0.16 | 1 | ||
| rs55730955 | 1.000 | 0.040 | 2 | 203721233 | intron variant | T/A | snv | 8.1E-02 | 1 | ||
| rs7367184 | 1.000 | 0.040 | 1 | 196891605 | intron variant | G/A | snv | 0.22 | 1 | ||
| rs16918167 | 1.000 | 0.040 | 9 | 99053057 | intron variant | G/T | snv | 0.29 | 1 | ||
| rs7712601 | 1.000 | 0.040 | 5 | 141538221 | intron variant | T/C | snv | 0.68 | 1 |