| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4769055 | 1.000 | 0.120 | 13 | 30735693 | intron variant | C/A | snv | 0.41 | 0.47 | 1 | |
| rs755403632 | 1.000 | 0.120 | 10 | 42792991 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs4919862 | 1.000 | 0.120 | 19 | 582253 | intron variant | T/C | snv | 0.82 | 1 | ||
| rs10780199 | 1.000 | 0.120 | 9 | 138058845 | intron variant | G/A | snv | 0.36 | 1 | ||
| rs7042521 | 1.000 | 0.120 | 9 | 137889440 | intron variant | C/G | snv | 0.31 | 1 | ||
| rs11137351 | 1.000 | 0.120 | 9 | 138045676 | intron variant | C/G | snv | 0.23 | 1 | ||
| rs2271875 | 1.000 | 0.120 | 19 | 3626924 | upstream gene variant | T/C | snv | 0.68 | 1 | ||
| rs2275235 | 1.000 | 0.120 | 1 | 150757803 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs774320676 | 1.000 | 0.120 | 1 | 150750091 | missense variant | A/T | snv | 4.0E-06 | 1 | ||
| rs928508030 | 1.000 | 0.120 | 1 | 150765698 | splice region variant | G/A | snv | 1 | |||
| rs1207570776 | 1.000 | 0.120 | 2 | 182757711 | missense variant | A/G | snv | 1 | |||
| rs4806942 | 1.000 | 0.120 | 19 | 3589341 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs1044006 | 1.000 | 0.120 | 19 | 15174241 | synonymous variant | T/A;C | snv | 0.86 | 1 | ||
| rs1044009 | 1.000 | 0.120 | 19 | 15160960 | missense variant | G/A | snv | 0.71 | 0.69 | 1 | |
| rs4382936 | 1.000 | 0.120 | 11 | 73241355 | non coding transcript exon variant | A/C | snv | 0.36 | 1 | ||
| rs4944832 | 1.000 | 0.120 | 11 | 73238127 | upstream gene variant | G/A;T | snv | 1 | |||
| rs13412 | 1.000 | 0.120 | 17 | 41811190 | missense variant | T/A;C | snv | 0.38 | 0.34 | 1 | |
| rs494860 | 1.000 | 0.120 | 13 | 113164695 | intron variant | T/A | snv | 0.26 | 0.19 | 1 | |
| rs2077777 | 1.000 | 0.120 | 4 | 26322296 | splice region variant | G/C | snv | 8.9E-02 | 1 | ||
| rs2270226 | 1.000 | 0.120 | 4 | 26415514 | missense variant | T/A;C;G | snv | 0.57 | 1 | ||
| rs35364374 | 1.000 | 0.120 | 19 | 38492540 | missense variant | G/T | snv | 6.9E-02 | 5.0E-02 | 1 | |
| rs56095120 | 1.000 | 0.120 | 22 | 31100540 | intron variant | T/A;C | snv | 1 | |||
| rs5997872 | 1.000 | 0.120 | 22 | 31095346 | missense variant | C/T | snv | 0.14 | 0.16 | 1 | |
| rs9621187 | 1.000 | 0.120 | 22 | 31103532 | non coding transcript exon variant | A/G | snv | 0.35 | 1 | ||
| rs4147064 | 1.000 | 0.120 | 13 | 30745981 | intron variant | T/C | snv | 0.50 | 2 |