| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 101 | ||
| rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 71 | ||
| rs752742313 | 0.637 | 0.320 | 3 | 138655502 | missense variant | C/T | snv | 1.2E-05 | 36 | ||
| rs568408 | 0.649 | 0.600 | 3 | 159995680 | 3 prime UTR variant | G/A | snv | 0.16 | 29 | ||
| rs1989839 | 0.790 | 0.160 | 3 | 50341515 | intron variant | A/G | snv | 0.22 | 0.20 | 8 | |
| rs1233296947 | 0.851 | 0.080 | 3 | 41225746 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
| rs121913282 | 0.882 | 0.040 | 3 | 179221072 | missense variant | A/C | snv | 4 | |||
| rs7646409 | 0.882 | 0.040 | 3 | 179182405 | intron variant | T/C | snv | 0.26 | 4 | ||
| rs2236947 | 0.882 | 0.040 | 3 | 50334001 | intron variant | C/A | snv | 0.39 | 3 | ||
| rs9866361 | 0.882 | 0.040 | 3 | 179190061 | intron variant | G/A | snv | 0.24 | 3 | ||
| rs10019009 | 0.851 | 0.080 | 4 | 87661983 | missense variant | A/G;T | snv | 4.0E-06; 0.29 | 4 | ||
| rs764191858 | 0.882 | 0.040 | 4 | 185502359 | missense variant | G/A | snv | 3 | |||
| rs3212227 | 0.566 | 0.840 | 5 | 159315942 | 3 prime UTR variant | T/G | snv | 0.26 | 65 | ||
| rs56149945 | 0.595 | 0.680 | 5 | 143399752 | missense variant | T/A;C | snv | 2.0E-02 | 49 | ||
| rs1800449 | 0.641 | 0.400 | 5 | 122077513 | missense variant | C/A;T | snv | 4.0E-06; 0.17 | 33 | ||
| rs368933511 | 0.851 | 0.080 | 5 | 179836485 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 5 | ||
| rs17206779 | 0.882 | 0.040 | 5 | 65151950 | splice region variant | C/G;T | snv | 0.48 | 3 | ||
| rs2010963 | 0.542 | 0.840 | 6 | 43770613 | 5 prime UTR variant | C/G | snv | 0.68 | 82 | ||
| rs699947 | 0.570 | 0.680 | 6 | 43768652 | upstream gene variant | A/C;T | snv | 67 | |||
| rs5370 | 0.630 | 0.520 | 6 | 12296022 | missense variant | G/T | snv | 0.23 | 0.21 | 37 | |
| rs745738344 | 0.653 | 0.600 | 6 | 31576786 | synonymous variant | G/A | snv | 1.6E-05 | 1.4E-05 | 28 | |
| rs12190287 | 0.708 | 0.280 | 6 | 133893387 | 3 prime UTR variant | C/G;T | snv | 19 | |||
| rs2070699 | 0.752 | 0.080 | 6 | 12292539 | intron variant | G/C;T | snv | 0.45 | 14 | ||
| rs1800541 | 0.851 | 0.120 | 6 | 12288986 | upstream gene variant | T/G | snv | 0.24 | 5 | ||
| rs1906953 | 0.882 | 0.040 | 6 | 34068669 | intron variant | C/T | snv | 0.25 | 4 |