| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2251177 | 1.000 | 0.040 | 3 | 114139503 | missense variant | C/A;T | snv | 8.0E-06; 0.99 | 1 | ||
| rs2267715 | 1.000 | 0.040 | 7 | 30676471 | intron variant | G/A;C | snv | 1 | |||
| rs3100127 | 1.000 | 0.040 | 1 | 202191842 | upstream gene variant | C/A;T | snv | 1 | |||
| rs363276 | 1.000 | 0.040 | 10 | 117274298 | intron variant | T/C;G | snv | 1 | |||
| rs406001 | 1.000 | 0.040 | 7 | 51938719 | intergenic variant | T/A;C | snv | 1 | |||
| rs451275 | 1.000 | 0.040 | 5 | 142392033 | intron variant | C/T | snv | 1 | |||
| rs58649573 | 1.000 | 0.040 | 9 | 124005148 | intron variant | T/C | snv | 1 | |||
| rs6812849 | 1.000 | 0.040 | 4 | 165951384 | intron variant | C/A;T | snv | 1 | |||
| rs717947 | 1.000 | 0.040 | 4 | 33652135 | intron variant | C/A;T | snv | 1 | |||
| rs7691872 | 1.000 | 0.040 | 4 | 165944433 | intron variant | G/C;T | snv | 1 | |||
| rs9868039 | 1.000 | 0.040 | 3 | 114127695 | 3 prime UTR variant | G/A;C | snv | 1 | |||
| rs1374141592 | 1.000 | 0.040 | 5 | 180630561 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs28363170 | 0.827 | 0.120 | 5 | 1393745 | 3 prime UTR variant | -/AGTGGGGGCCCTGCATGCGTCCTGGGGTAGTACACGCTCC | delins | 8.1E-06 | 7 | ||
| rs1801028 | 0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 | 24 | |
| rs10144436 | 1.000 | 0.040 | 14 | 95090065 | 3 prime UTR variant | C/A | snv | 2.9E-02 | 1 | ||
| rs12898919 | 1.000 | 0.040 | 15 | 78588235 | intron variant | G/C | snv | 3.1E-02 | 1 | ||
| rs2075652 | 1.000 | 0.040 | 11 | 113424176 | intron variant | G/A | snv | 4.2E-02 | 1 | ||
| rs56242606 | 1.000 | 0.040 | 7 | 12382283 | intron variant | T/C | snv | 5.3E-02 | 2 | ||
| rs12364283 | 0.925 | 0.080 | 11 | 113476233 | upstream gene variant | A/G | snv | 5.8E-02 | 3 | ||
| rs16904179 | 1.000 | 0.040 | 8 | 129946705 | intron variant | G/A | snv | 6.2E-02 | 1 | ||
| rs17759843 | 0.882 | 0.080 | 22 | 21920372 | 3 prime UTR variant | G/A | snv | 6.7E-02 | 4 | ||
| rs263232 | 1.000 | 0.040 | 8 | 130795923 | intron variant | C/A | snv | 6.7E-02 | 1 | ||
| rs696217 | 0.662 | 0.640 | 3 | 10289773 | missense variant | G/T | snv | 8.8E-02 | 7.1E-02 | 32 | |
| rs28932171 | 1.000 | 0.040 | 10 | 60071532 | missense variant | T/C | snv | 7.2E-02 | 7.3E-02 | 1 | |
| rs11599164 | 1.000 | 0.040 | 10 | 60072226 | missense variant | G/T | snv | 7.2E-02 | 7.3E-02 | 1 |