| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10801531 | 1.000 | 0.040 | 1 | 196394414 | intron variant | G/A | snv | 0.27 | 2 | ||
| rs10801532 | 1.000 | 0.040 | 1 | 196395046 | intron variant | A/G;T | snv | 2 | |||
| rs10801537 | 1.000 | 0.040 | 1 | 196457711 | intron variant | A/G | snv | 0.33 | 2 | ||
| rs10801551 | 1.000 | 0.040 | 1 | 196610909 | upstream gene variant | G/A;C | snv | 2 | |||
| rs10801553 | 1.000 | 0.040 | 1 | 196686613 | intron variant | A/C | snv | 0.64 | 1 | ||
| rs10801554 | 1.000 | 0.040 | 1 | 196688525 | intron variant | C/T | snv | 0.64 | 1 | ||
| rs10801555 | 1.000 | 0.040 | 1 | 196691131 | intron variant | A/G | snv | 0.64 | 1 | ||
| rs10801556 | 1.000 | 0.040 | 1 | 196691334 | intron variant | A/G | snv | 0.64 | 1 | ||
| rs10801560 | 1.000 | 0.040 | 1 | 196745470 | intron variant | C/A | snv | 0.19 | 2 | ||
| rs10801561 | 1.000 | 0.040 | 1 | 196745540 | intron variant | T/A | snv | 0.19 | 2 | ||
| rs10801575 | 1.000 | 0.040 | 1 | 196883651 | intron variant | T/A;C | snv | 1 | |||
| rs10801580 | 1.000 | 0.040 | 1 | 196916555 | non coding transcript exon variant | T/C | snv | 0.21 | 1 | ||
| rs10887142 | 1.000 | 0.040 | 10 | 122347969 | downstream gene variant | G/A;C | snv | 1 | |||
| rs10887149 | 1.000 | 0.040 | 10 | 122407488 | intron variant | G/A;C | snv | 1 | |||
| rs10887150 | 1.000 | 0.040 | 10 | 122421062 | non coding transcript exon variant | C/A | snv | 0.47 | 1 | ||
| rs10887151 | 1.000 | 0.040 | 10 | 122421250 | non coding transcript exon variant | C/T | snv | 0.45 | 1 | ||
| rs10922071 | 1.000 | 0.040 | 1 | 196464740 | intron variant | G/A | snv | 0.33 | 2 | ||
| rs10922082 | 1.000 | 0.040 | 1 | 196544564 | intron variant | G/A | snv | 0.30 | 1 | ||
| rs10922083 | 1.000 | 0.040 | 1 | 196547268 | intron variant | C/A;T | snv | 1 | |||
| rs10922084 | 1.000 | 0.040 | 1 | 196556184 | intron variant | A/C | snv | 0.30 | 1 | ||
| rs10922094 | 1.000 | 0.040 | 1 | 196692375 | intron variant | G/C;T | snv | 1 | |||
| rs10922096 | 1.000 | 0.040 | 1 | 196693329 | intron variant | T/C | snv | 0.41 | 1 | ||
| rs10922102 | 1.000 | 0.040 | 1 | 196699157 | intron variant | C/T | snv | 0.64 | 1 | ||
| rs10922106 | 0.925 | 0.080 | 1 | 196722334 | intron variant | A/G | snv | 0.43 | 2 | ||
| rs10922144 | 1.000 | 0.040 | 1 | 196854170 | intron variant | C/A;T | snv | 2 |