| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1046089 | 0.882 | 0.200 | 6 | 31635190 | missense variant | G/A | snv | 0.36 | 0.40 | 4 | |
| rs10466455 | 1.000 | 0.080 | 11 | 34759389 | intergenic variant | T/C | snv | 0.39 | 1 | ||
| rs1048257 | 1.000 | 0.080 | 14 | 104938047 | 3 prime UTR variant | T/C;G | snv | 0.54 | 1 | ||
| rs10484399 | 0.851 | 0.240 | 6 | 27566749 | intergenic variant | A/G | snv | 5.4E-02 | 4 | ||
| rs1048801 | 1.000 | 0.080 | 19 | 54667913 | missense variant | G/A;C;T | snv | 1 | |||
| rs10488631 | 0.742 | 0.280 | 7 | 128954129 | upstream gene variant | T/C | snv | 9.0E-02 | 13 | ||
| rs10489265 | 0.827 | 0.200 | 1 | 173266926 | regulatory region variant | A/C | snv | 0.21 | 5 | ||
| rs104895257 | 1.000 | 0.080 | 12 | 6333441 | missense variant | C/T | snv | 4.0E-05 | 7.0E-06 | 1 | |
| rs1048971 | 0.851 | 0.160 | 1 | 207472977 | synonymous variant | G/A;T | snv | 0.34; 8.0E-06 | 4 | ||
| rs10491322 | 0.925 | 0.120 | 5 | 134194449 | 3 prime UTR variant | A/G | snv | 9.5E-02 | 3 | ||
| rs1049564 | 0.882 | 0.160 | 14 | 20472447 | missense variant | G/A | snv | 0.19 | 0.21 | 6 | |
| rs10496105 | 1.000 | 0.080 | 2 | 64093612 | 3 prime UTR variant | G/A | snv | 0.11 | 1 | ||
| rs10498070 | 0.925 | 0.080 | 2 | 219833404 | intergenic variant | A/C | snv | 0.39 | 2 | ||
| rs10499194 | 0.752 | 0.400 | 6 | 137681500 | intron variant | C/T | snv | 0.24 | 10 | ||
| rs10499197 | 0.925 | 0.080 | 6 | 137811379 | intergenic variant | T/G | snv | 2.4E-02 | 2 | ||
| rs1050499 | 1.000 | 0.080 | 1 | 161673197 | missense variant | A/T | snv | 2.4E-03 | 4.4E-03 | 1 | |
| rs1050501 | 0.732 | 0.440 | 1 | 161674008 | missense variant | T/C | snv | 0.16 | 0.19 | 15 | |
| rs1051169 | 0.851 | 0.200 | 21 | 46602317 | synonymous variant | C/A;G;T | snv | 0.65 | 5 | ||
| rs10515746 | 0.925 | 0.240 | 5 | 157109557 | intron variant | A/C;T | snv | 2 | |||
| rs10516487 | 0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 | 11 | ||
| rs1051792 | 0.851 | 0.240 | 6 | 31411200 | missense variant | G/A | snv | 0.34 | 0.35 | 5 | |
| rs1052231 | 1.000 | 0.080 | 1 | 167430837 | 3 prime UTR variant | T/A | snv | 0.82 | 1 | ||
| rs1053874 | 0.851 | 0.240 | 16 | 3657746 | missense variant | G/A;T | snv | 0.36; 4.0E-06 | 7 | ||
| rs1057108 | 1.000 | 0.080 | 10 | 35196021 | 5 prime UTR variant | T/G | snv | 0.34 | 0.34 | 1 | |
| rs1059312 | 1.000 | 0.080 | 12 | 128794319 | synonymous variant | A/G | snv | 0.44 | 0.43 | 1 |