| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1011970 | 0.677 | 0.320 | 9 | 22062135 | intron variant | G/T | snv | 0.23 | 1 | ||
| rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 7 | |
| rs10519198 | 0.925 | 0.080 | 15 | 78450412 | intron variant | C/A;G | snv | 2 | |||
| rs1062980 | 0.827 | 0.080 | 15 | 78500185 | 3 prime UTR variant | T/C | snv | 0.39 | 4 | ||
| rs10937405 | 0.807 | 0.080 | 3 | 189665394 | intron variant | C/T | snv | 0.38 | 1 | ||
| rs11235604 | 0.925 | 0.080 | 11 | 72822491 | missense variant | C/T | snv | 7.0E-03 | 2.3E-03 | 1 | |
| rs1150752 | 0.882 | 0.240 | 6 | 32096949 | missense variant | T/C;G | snv | 5.9E-02 | 3 | ||
| rs11571833 | 0.608 | 0.360 | 13 | 32398489 | stop gained | A/T | snv | 6.6E-03 | 6.0E-03 | 2 | |
| rs11638372 | 0.925 | 0.080 | 15 | 78691217 | intron variant | C/A;G;T | snv | 0.28 | 3 | ||
| rs11639372 | 0.925 | 0.080 | 15 | 78674313 | intron variant | C/T | snv | 0.30 | 1 | ||
| rs1235162 | 0.827 | 0.280 | 6 | 29569447 | intron variant | A/G | snv | 6.0E-02 | 6 | ||
| rs12441998 | 0.925 | 0.080 | 15 | 78637030 | intron variant | G/A | snv | 0.63 | 3 | ||
| rs12503223 | 1.000 | 0.040 | 4 | 16841093 | intron variant | G/A | snv | 0.18 | 1 | ||
| rs12594247 | 0.925 | 0.080 | 15 | 78654291 | intron variant | C/T | snv | 0.14 | 3 | ||
| rs1270942 | 0.742 | 0.440 | 6 | 31951083 | non coding transcript exon variant | A/G | snv | 7.5E-02 | 6 | ||
| rs12910984 | 0.827 | 0.080 | 15 | 78599285 | intron variant | G/A;C;T | snv | 3 | |||
| rs12914385 | 0.790 | 0.160 | 15 | 78606381 | intron variant | C/A;T | snv | 8 | |||
| rs1316971 | 0.925 | 0.080 | 15 | 78638168 | intron variant | A/G;T | snv | 0.62 | 3 | ||
| rs13180 | 0.851 | 0.160 | 15 | 78497146 | synonymous variant | C/T | snv | 0.54 | 0.51 | 4 | |
| rs13314271 | 0.925 | 0.080 | 3 | 189639813 | intron variant | T/C | snv | 0.45 | 1 | ||
| rs1394371 | 0.925 | 0.080 | 15 | 78432127 | intergenic variant | C/T | snv | 0.22 | 3 | ||
| rs16969968 | 0.653 | 0.360 | 15 | 78590583 | missense variant | G/A | snv | 0.26 | 0.24 | 1 | |
| rs16970006 | 1.000 | 0.040 | 15 | 78677917 | intron variant | T/C | snv | 8.7E-02 | 2 | ||
| rs17391694 | 0.882 | 0.120 | 1 | 78157942 | regulatory region variant | C/T | snv | 7.8E-02 | 3 | ||
| rs17487514 | 0.925 | 0.080 | 15 | 78661443 | non coding transcript exon variant | C/T | snv | 0.19 | 3 |