| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1033180 | 1.000 | 0.080 | 6 | 383546 | regulatory region variant | C/T | snv | 5.4E-02 | 1 | ||
| rs10796045 | 1.000 | 0.080 | 10 | 6360779 | intergenic variant | G/T | snv | 0.79 | 1 | ||
| rs10886159 | 1.000 | 0.080 | 10 | 117854099 | intergenic variant | T/C | snv | 0.25 | 1 | ||
| rs11100722 | 1.000 | 0.080 | 4 | 141616307 | intergenic variant | G/C | snv | 0.77 | 1 | ||
| rs12142280 | 1.000 | 0.080 | 1 | 172895512 | intron variant | T/A | snv | 0.21 | 1 | ||
| rs12727642 | 1.000 | 0.080 | 1 | 7986612 | upstream gene variant | C/A | snv | 0.12 | 1 | ||
| rs1378938 | 1.000 | 0.080 | 15 | 74804102 | downstream gene variant | T/A;C | snv | 1 | |||
| rs1997179 | 1.000 | 0.080 | 4 | 122063478 | intergenic variant | T/C | snv | 0.21 | 1 | ||
| rs2097282 | 1.000 | 0.080 | 3 | 46336534 | intergenic variant | C/T | snv | 0.68 | 1 | ||
| rs2157453 | 1.000 | 0.080 | 1 | 172894808 | intron variant | G/A | snv | 0.31 | 1 | ||
| rs2187670 | 1.000 | 0.080 | 3 | 46325463 | intergenic variant | T/C | snv | 0.81 | 1 | ||
| rs4558075 | 1.000 | 0.080 | 10 | 6359663 | intergenic variant | C/A;G;T | snv | 1 | |||
| rs4899260 | 1.000 | 0.080 | 14 | 68811487 | intergenic variant | C/T | snv | 0.28 | 1 | ||
| rs4946111 | 1.000 | 0.080 | 6 | 115663255 | intergenic variant | T/A;G | snv | 1 | |||
| rs4956400 | 1.000 | 0.080 | 4 | 141556189 | intergenic variant | T/C | snv | 0.75 | 1 | ||
| rs62184863 | 1.000 | 0.080 | 2 | 203819074 | intergenic variant | G/C | snv | 6.2E-02 | 1 | ||
| rs6762743 | 1.000 | 0.080 | 3 | 179294212 | intergenic variant | C/T | snv | 0.29 | 1 | ||
| rs7104791 | 1.000 | 0.080 | 11 | 111326133 | downstream gene variant | T/A;C | snv | 1 | |||
| rs77027760 | 1.000 | 0.080 | 6 | 137680924 | intron variant | G/A | snv | 0.15 | 1 | ||
| rs859715 | 1.000 | 0.080 | 1 | 172790982 | intron variant | A/T | snv | 0.36 | 1 | ||
| rs9391227 | 1.000 | 0.080 | 6 | 104710759 | regulatory region variant | T/A | snv | 0.56 | 1 | ||
| rs971290 | 1.000 | 0.080 | 14 | 68805252 | intergenic variant | C/A;G;T | snv | 1 | |||
| rs8081319 | 1.000 | 0.080 | 17 | 37374139 | intron variant | A/G | snv | 6.8E-02 | 1 | ||
| rs61579022 | 1.000 | 0.080 | 3 | 119404431 | intron variant | G/A | snv | 0.30 | 1 | ||
| rs7753008 | 1.000 | 0.080 | 6 | 90099920 | intron variant | T/A;C | snv | 1 |