| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7500448 | 1.000 | 0.040 | 16 | 83012185 | intron variant | A/G | snv | 0.20 | 3 | ||
| rs10806235 | 1.000 | 0.040 | 6 | 81993618 | intron variant | C/T | snv | 0.31 | 1 | ||
| rs4613862 | 1.000 | 0.040 | 6 | 81902554 | intron variant | A/C | snv | 0.37 | 1 | ||
| rs7199941 | 1.000 | 0.040 | 16 | 81872818 | intron variant | A/G;T | snv | 1 | |||
| rs7342694 | 1.000 | 0.040 | 16 | 81870195 | intron variant | T/C | snv | 0.55 | 1 | ||
| rs78707197 | 1.000 | 0.040 | 6 | 81749317 | 3 prime UTR variant | T/C | snv | 1.3E-02 | 1 | ||
| rs11099493 | 1.000 | 0.040 | 4 | 81665896 | intron variant | A/C;G | snv | 1 | |||
| rs11556218 | 0.653 | 0.600 | 15 | 81305928 | missense variant | T/G | snv | 9.6E-02 | 0.12 | 1 | |
| rs12264252 | 1.000 | 0.040 | 10 | 80517585 | intron variant | G/A | snv | 0.18 | 1 | ||
| rs17680741 | 1.000 | 0.040 | 10 | 80491758 | intron variant | T/C | snv | 0.25 | 1 | ||
| rs10857147 | 1.000 | 0.040 | 4 | 80259918 | intergenic variant | A/T | snv | 0.25 | 9 | ||
| rs7173743 | 0.851 | 0.120 | 15 | 78849442 | intron variant | T/C | snv | 0.45 | 2 | ||
| rs11637783 | 1.000 | 0.040 | 15 | 78846658 | intron variant | T/C | snv | 0.34 | 1 | ||
| rs11072811 | 1.000 | 0.040 | 15 | 78839988 | intron variant | A/C | snv | 0.51 | 1 | ||
| rs4468572 | 1.000 | 0.040 | 15 | 78832133 | intron variant | T/C | snv | 0.58 | 1 | ||
| rs7164479 | 1.000 | 0.040 | 15 | 78830712 | intron variant | C/T | snv | 0.58 | 1 | ||
| rs6495335 | 1.000 | 0.040 | 15 | 78824791 | intron variant | G/T | snv | 0.63 | 1 | ||
| rs3825807 | 0.807 | 0.120 | 15 | 78796769 | missense variant | A/G | snv | 0.34 | 0.33 | 2 | |
| rs1994016 | 0.851 | 0.160 | 15 | 78787892 | intron variant | C/T | snv | 0.30 | 1 | ||
| rs12500824 | 1.000 | 0.040 | 4 | 76495474 | intron variant | A/G;T | snv | 3 | |||
| rs1135889 | 1.000 | 0.040 | 17 | 75930040 | missense variant | C/A | snv | 0.19 | 0.21 | 1 | |
| rs659418 | 1.000 | 0.040 | 11 | 75573289 | downstream gene variant | T/G | snv | 0.19 | 2 | ||
| rs606452 | 1.000 | 0.040 | 11 | 75565133 | intron variant | A/C | snv | 0.78 | 3 | ||
| rs590121 | 1.000 | 0.040 | 11 | 75563105 | 5 prime UTR variant | G/T | snv | 0.36 | 1 | ||
| rs12930452 | 1.000 | 0.040 | 16 | 75428157 | intron variant | A/G | snv | 0.51 | 1 |