| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7521584 | 1.000 | 0.040 | 1 | 1168578 | upstream gene variant | T/A;G | snv | 3 | |||
| rs1042194 | 1.000 | 0.040 | 10 | 94735727 | 3 prime UTR variant | G/C;T | snv | 2 | |||
| rs10505799 | 1.000 | 0.040 | 12 | 16293334 | intergenic variant | T/C | snv | 0.10 | 2 | ||
| rs2014486 | 1.000 | 0.040 | 11 | 1237573 | intron variant | A/G | snv | 0.52 | 2 | ||
| rs2920283 | 0.925 | 0.040 | 8 | 142675619 | intron variant | T/C | snv | 0.44 | 2 | ||
| rs6878265 | 1.000 | 0.040 | 5 | 120069960 | intergenic variant | C/T | snv | 0.29 | 2 | ||
| rs12423190 | 1.000 | 0.040 | 12 | 112471536 | intron variant | T/C | snv | 8.7E-02 | 1 | ||
| rs1440526066 | 1.000 | 0.040 | 5 | 132679827 | missense variant | G/A | snv | 1 | |||
| rs1886753 | 1.000 | 0.040 | 6 | 40359357 | non coding transcript exon variant | C/T | snv | 0.42 | 1 | ||
| rs61516247 | 1.000 | 0.040 | 6 | 40344500 | non coding transcript exon variant | G/A | snv | 0.17 | 1 | ||
| rs7481521 | 1.000 | 0.040 | 11 | 1027811 | missense variant | C/T | snv | 0.50 | 0.47 | 1 | |
| rs764097618 | 1.000 | 0.040 | 16 | 27360794 | splice donor variant | G/A | snv | 4.0E-06 | 1 | ||
| rs765803011 | 1.000 | 0.040 | 16 | 27363094 | missense variant | C/G;T | snv | 4.0E-06; 1.6E-05 | 1 | ||
| rs7747696 | 1.000 | 0.040 | 6 | 42093217 | non coding transcript exon variant | A/G | snv | 0.54 | 1 | ||
| rs7749023 | 1.000 | 0.040 | 6 | 42093995 | non coding transcript exon variant | A/C;T | snv | 1 | |||
| rs9315542 | 1.000 | 0.040 | 13 | 38057334 | intron variant | T/C | snv | 0.26 | 1 | ||
| rs9471643 | 0.882 | 0.080 | 6 | 41751177 | intron variant | G/C | snv | 0.19 | 6 | ||
| rs10739971 | 0.882 | 0.080 | 9 | 94175398 | intron variant | G/A;C | snv | 5 | |||
| rs1002765 | 0.851 | 0.080 | 3 | 87227912 | intron variant | G/A;C | snv | 4 | |||
| rs121224 | 0.851 | 0.080 | 17 | 31574981 | intron variant | G/C | snv | 0.66 | 4 | ||
| rs6458238 | 0.882 | 0.080 | 6 | 41749967 | intron variant | G/A;C | snv | 4 | |||
| rs158916 | 0.882 | 0.080 | 5 | 60949318 | intron variant | A/G | snv | 0.15 | 3 | ||
| rs2029298 | 0.882 | 0.080 | 11 | 47213167 | upstream gene variant | C/T | snv | 0.62 | 3 | ||
| rs254942 | 0.882 | 0.080 | 16 | 13932150 | splice region variant | G/A;C;T | snv | 0.97; 4.0E-06; 4.0E-06 | 3 | ||
| rs326222 | 0.882 | 0.080 | 11 | 47238117 | intron variant | T/C | snv | 0.60 | 0.58 | 3 |