| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs708494 | 1.000 | 0.040 | 14 | 52300623 | regulatory region variant | G/A | snv | 0.47 | 2 | ||
| rs140570886 | 1.000 | 0.040 | 6 | 160591981 | intron variant | T/C | snv | 2.8E-02 | 3 | ||
| rs1790349 | 0.882 | 0.040 | 11 | 71431304 | intron variant | T/C | snv | 0.19 | 4 | ||
| rs2291725 | 0.882 | 0.120 | 17 | 48961770 | missense variant | T/C | snv | 0.50 | 0.40 | 4 | |
| rs36071027 | 0.925 | 0.080 | 5 | 159017266 | intron variant | C/T | snv | 0.29 | 4 | ||
| rs2048327 | 0.851 | 0.120 | 6 | 160442500 | intron variant | T/C | snv | 0.28 | 5 | ||
| rs763802417 | 0.882 | 0.040 | X | 100862805 | missense variant | G/A | snv | 5.9E-06 | 5 | ||
| rs7692387 | 0.925 | 0.080 | 4 | 155714157 | intron variant | G/A | snv | 0.16 | 5 | ||
| rs12746200 | 0.851 | 0.160 | 1 | 186880054 | intron variant | A/G | snv | 7.3E-02 | 6 | ||
| rs1537375 | 0.882 | 0.120 | 9 | 22116072 | intron variant | T/C;G | snv | 6 | |||
| rs74830677 | 0.882 | 0.080 | 12 | 124800125 | missense variant | G/A | snv | 9.9E-04 | 6.7E-04 | 6 | |
| rs10116277 | 0.827 | 0.160 | 9 | 22081398 | intron variant | G/T | snv | 0.62 | 8 | ||
| rs10903323 | 0.807 | 0.160 | 8 | 10292057 | intron variant | A/G | snv | 0.15 | 8 | ||
| rs1282382243 | 0.807 | 0.120 | 13 | 50843630 | missense variant | G/A | snv | 8 | |||
| rs17608766 | 1.000 | 0.040 | 17 | 46935905 | 3 prime UTR variant | T/C | snv | 9.2E-02 | 8 | ||
| rs532019808 | 0.827 | 0.120 | 11 | 89451807 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 8 | ||
| rs1866389 | 0.790 | 0.080 | 5 | 80065442 | missense variant | G/C | snv | 0.17 | 0.17 | 9 | |
| rs3732581 | 0.790 | 0.120 | 3 | 183840614 | missense variant | C/G;T | snv | 0.46; 1.2E-05 | 9 | ||
| rs544456198 | 0.790 | 0.120 | 19 | 11116930 | missense variant | G/T | snv | 8.0E-06 | 2.8E-05 | 9 | |
| rs604723 | 1.000 | 0.040 | 11 | 100739815 | intron variant | T/C | snv | 0.78 | 9 | ||
| rs6700896 | 0.827 | 0.160 | 1 | 65624099 | intron variant | C/T | snv | 0.44 | 9 | ||
| rs6850 | 0.790 | 0.160 | 7 | 44796715 | 5 prime UTR variant | A/G;T | snv | 0.26; 4.0E-06 | 9 | ||
| rs6905288 | 0.882 | 0.120 | 6 | 43791136 | downstream gene variant | G/A | snv | 0.56 | 9 | ||
| rs911119 | 0.807 | 0.120 | 20 | 23632100 | non coding transcript exon variant | C/G;T | snv | 9 | |||
| rs9818870 | 0.807 | 0.200 | 3 | 138403280 | 3 prime UTR variant | C/A;T | snv | 9 |