| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs374524467 | 0.827 | 0.040 | 4 | 110632961 | missense variant | A/C | snv | 8.0E-06 | 7.0E-06 | 5 | |
| rs4938723 | 0.574 | 0.680 | 11 | 111511840 | intron variant | T/C | snv | 0.32 | 60 | ||
| rs12241008 | 0.716 | 0.160 | 10 | 112520943 | intron variant | T/C | snv | 0.13 | 16 | ||
| rs10506868 | 0.716 | 0.160 | 10 | 112559621 | intron variant | C/T | snv | 3.1E-02 | 16 | ||
| rs11599775 | 1.000 | 0.040 | 10 | 112699938 | intron variant | G/A | snv | 0.27 | 2 | ||
| rs11196067 | 0.752 | 0.160 | 10 | 112709306 | intron variant | A/T | snv | 0.32 | 10 | ||
| rs11196172 | 0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 | 18 | ||
| rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 93 | |||
| rs7904519 | 0.763 | 0.240 | 10 | 113014168 | intron variant | A/G | snv | 0.55 | 9 | ||
| rs648044 | 0.882 | 0.040 | 11 | 114160077 | non coding transcript exon variant | A/G;T | snv | 4 | |||
| rs17138945 | 1.000 | 0.040 | 7 | 116703812 | intron variant | T/G | snv | 7.3E-02 | 1 | ||
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 93 | |
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs498872 | 0.776 | 0.240 | 11 | 118606652 | 5 prime UTR variant | A/G;T | snv | 10 | |||
| rs12803321 | 1.000 | 0.040 | 11 | 118609400 | intron variant | G/C;T | snv | 2 | |||
| rs11603023 | 0.925 | 0.120 | 11 | 118615352 | intron variant | T/C | snv | 0.57 | 3 | ||
| rs11216930 | 1.000 | 0.040 | 11 | 118618067 | intron variant | A/C | snv | 0.22 | 2 | ||
| rs2236661 | 1.000 | 0.040 | 11 | 118628678 | intron variant | C/G | snv | 0.24 | 0.20 | 1 | |
| rs494560 | 1.000 | 0.040 | 11 | 118650844 | non coding transcript exon variant | A/G | snv | 0.57 | 1 | ||
| rs17748 | 0.827 | 0.080 | 11 | 118657714 | 3 prime UTR variant | C/T | snv | 0.18 | 5 | ||
| rs11216943 | 1.000 | 0.040 | 11 | 118685689 | downstream gene variant | G/A | snv | 0.20 | 1 | ||
| rs573905 | 1.000 | 0.040 | 11 | 118701558 | intron variant | A/G | snv | 0.56 | 1 | ||
| rs10892258 | 0.925 | 0.120 | 11 | 118709156 | intron variant | G/A | snv | 0.19 | 4 | ||
| rs643788 | 1.000 | 0.040 | 11 | 119097048 | missense variant | T/C | snv | 0.42 | 0.38 | 1 |