| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17070145 | 0.790 | 0.120 | 5 | 168418786 | intron variant | C/T | snv | 0.43 | 10 | ||
| rs387906789 | 0.742 | 0.200 | 9 | 35065352 | missense variant | G/A;C | snv | 4.0E-06 | 14 | ||
| rs121909330 | 0.752 | 0.200 | 9 | 35065364 | missense variant | G/A;C;T | snv | 11 | |||
| rs121909334 | 0.752 | 0.200 | 9 | 35065255 | missense variant | C/T | snv | 1.6E-05 | 10 | ||
| rs387906709 | 0.776 | 0.120 | X | 56565363 | missense variant | C/A;T | snv | 9 | |||
| rs121918100 | 0.827 | 0.160 | 18 | 31595184 | missense variant | T/C | snv | 11 | |||
| rs766647311 | 0.882 | 0.080 | 6 | 41159841 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
| rs797044603 | 0.827 | 0.320 | 6 | 41161541 | missense variant | T/C | snv | 4.0E-06 | 5 | ||
| rs2306604 | 0.827 | 0.080 | 10 | 58388932 | intron variant | A/C;G;T | snv | 5 | |||
| rs367543041 | 0.742 | 0.200 | 1 | 11022553 | missense variant | G/A;C | snv | 3.0E-05 | 15 | ||
| rs80356715 | 0.807 | 0.120 | 1 | 11016874 | missense variant | C/G;T | snv | 8.0E-06; 2.2E-04 | 6 | ||
| rs2618516 | 0.882 | 0.080 | 11 | 14000092 | intron variant | T/C | snv | 0.65 | 3 | ||
| rs12976445 | 0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 | 20 | ||
| rs2298813 | 0.790 | 0.120 | 11 | 121522975 | missense variant | G/A;T | snv | 7.2E-02; 4.0E-06 | 7 | ||
| rs1010159 | 0.882 | 0.080 | 11 | 121612692 | non coding transcript exon variant | C/T | snv | 0.55 | 0.55 | 3 | |
| rs3824968 | 0.925 | 0.080 | 11 | 121605213 | synonymous variant | T/A | snv | 0.39 | 0.29 | 2 | |
| rs11931074 | 0.851 | 0.080 | 4 | 89718364 | intron variant | G/A;C;T | snv | 7 | |||
| rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
| rs104893875 | 0.742 | 0.120 | 4 | 89828170 | missense variant | C/T | snv | 4.0E-06 | 13 | ||
| rs201106962 | 0.851 | 0.080 | 4 | 89828156 | missense variant | A/C | snv | 8.0E-05 | 7.0E-05 | 5 | |
| rs1043202 | 0.882 | 0.080 | 12 | 54182178 | missense variant | T/A | snv | 3 | |||
| rs1741309 | 1.000 | 0.080 | 20 | 4163930 | intron variant | A/G | snv | 0.53 | 1 | ||
| rs6347 | 0.851 | 0.080 | 5 | 1411297 | synonymous variant | T/C | snv | 0.23 | 0.32 | 4 | |
| rs4879809 | 0.882 | 0.120 | 9 | 34635601 | 3 prime UTR variant | T/A;C;G | snv | 1.1E-03; 1.00 | 3 | ||
| rs63750215 | 0.701 | 0.240 | 1 | 226885603 | missense variant | A/T | snv | 19 |