| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 19 | ||
| rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 10 | ||
| rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 9 | ||
| rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 9 | ||
| rs333947 | 1 | 109928142 | intron variant | G/A | snv | 0.13 | 7 | ||||
| rs12748152 | 1.000 | 0.120 | 1 | 26811902 | upstream gene variant | C/T | snv | 5.7E-02 | 6 | ||
| rs2642438 | 1 | 220796686 | missense variant | A/G | snv | 0.75 | 0.78 | 6 | |||
| rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 6 | |||
| rs114165349 | 1 | 26695422 | intron variant | G/C | snv | 1.7E-02 | 5 | ||||
| rs3768321 | 1.000 | 0.080 | 1 | 39570256 | intron variant | G/T | snv | 0.14 | 5 | ||
| rs79598313 | 1 | 26958422 | intron variant | C/A;T | snv | 5 | |||||
| rs1011731 | 1 | 172377408 | intron variant | G/A | snv | 0.46 | 4 | ||||
| rs10127775 | 1 | 230160042 | intron variant | A/G;T | snv | 4 | |||||
| rs10900522 | 1 | 205714939 | 3 prime UTR variant | T/C | snv | 0.21 | 4 | ||||
| rs2296172 | 1.000 | 0.080 | 1 | 39370145 | missense variant | A/G;T | snv | 0.19; 8.0E-06 | 4 | ||
| rs267738 | 1.000 | 0.040 | 1 | 150968149 | missense variant | T/A;G | snv | 4.0E-06; 0.15 | 4 | ||
| rs4495740 | 1 | 62658794 | intron variant | T/G | snv | 0.34 | 4 | ||||
| rs4660293 | 1 | 39562508 | non coding transcript exon variant | A/C;G | snv | 4 | |||||
| rs10864728 | 1 | 230169168 | intron variant | A/G | snv | 0.50 | 3 | ||||
| rs12133576 | 1.000 | 0.040 | 1 | 93350843 | intron variant | A/G | snv | 0.51 | 3 | ||
| rs12145743 | 1 | 156730859 | intron variant | T/G | snv | 0.24 | 3 | ||||
| rs1689788 | 1 | 182175287 | intron variant | T/C | snv | 0.29 | 3 | ||||
| rs193084249 | 1 | 26661155 | intergenic variant | A/G | snv | 1.7E-02 | 3 | ||||
| rs3902354 | 1 | 109276674 | downstream gene variant | C/A;T | snv | 3 | |||||
| rs4847240 | 1 | 93352389 | intron variant | A/G | snv | 0.51 | 3 |