| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1360182594 | 1 | 11790755 | synonymous variant | G/A | snv | 4.0E-06 | 1 | ||||
| rs915014 | 0.925 | 0.040 | 1 | 11789412 | missense variant | T/C | snv | 2 | |||
| rs145641996 | 1.000 | 0.040 | 1 | 11792285 | missense variant | T/C;G | snv | 1.6E-05; 1.6E-04 | 2 | ||
| rs17367504 | 1.000 | 0.040 | 1 | 11802721 | intron variant | A/G | snv | 0.14 | 2 | ||
| rs13306560 | 1.000 | 0.040 | 1 | 11806126 | 5 prime UTR variant | C/T | snv | 3.7E-02 | 2 | ||
| rs760161369 | 0.882 | 0.040 | 1 | 11800214 | missense variant | G/A;C | snv | 2.8E-05; 4.0E-06 | 2 | ||
| rs121434296 | 0.882 | 0.040 | 1 | 11794766 | missense variant | G/A | snv | 2.0E-05 | 3.5E-05 | 1 | |
| rs202095816 | 1.000 | 0.040 | 1 | 11801254 | missense variant | T/C | snv | 1.6E-05 | 1.4E-05 | 1 | |
| rs17421511 | 1.000 | 0.040 | 1 | 11797731 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs1203757587 | 1.000 | 0.040 | 1 | 11792279 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs761230732 | 1.000 | 0.040 | 1 | 11801211 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
| rs1314498183 | 1.000 | 0.040 | 1 | 11803469 | missense variant | G/A | snv | 4.2E-06 | 1 | ||
| rs774321998 | 1.000 | 0.040 | 1 | 11790683 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1374061192 | 1.000 | 0.040 | 1 | 11801186 | synonymous variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1200746244 | 0.807 | 0.080 | 1 | 11801287 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 11 | |
| rs3753584 | 0.827 | 0.080 | 1 | 11804529 | 5 prime UTR variant | T/C | snv | 0.14 | 5 | ||
| rs114673809 | 0.882 | 0.080 | 1 | 11787703 | 3 prime UTR variant | G/A | snv | 5.0E-03 | 3 | ||
| rs781742574 | 0.882 | 0.080 | 1 | 11800254 | missense variant | T/C | snv | 4.0E-06 | 3 | ||
| rs200100285 | 0.851 | 0.080 | 1 | 11796313 | missense variant | T/C;G | snv | 1.9E-04 | 3 | ||
| rs765167328 | 1.000 | 0.080 | 1 | 11803027 | synonymous variant | C/T | snv | 1.6E-05 | 4.2E-05 | 1 | |
| rs150963282 | 1.000 | 0.080 | 1 | 11800285 | synonymous variant | G/T | snv | 9.9E-05 | 1.9E-04 | 1 | |
| rs373524607 | 1.000 | 0.080 | 1 | 11794397 | synonymous variant | A/G | snv | 1.2E-05 | 1 | ||
| rs147257424 | 0.925 | 0.080 | 1 | 11801299 | missense variant | C/A;G;T | snv | 1.2E-05; 1.2E-05 | 1 | ||
| rs768248826 | 1.000 | 0.080 | 1 | 11801265 | missense variant | G/A;C | snv | 8.0E-06 | 1 | ||
| rs775254308 | 1.000 | 0.080 | 1 | 11803451 | missense variant | C/T | snv | 4.2E-06 | 1 |