| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6020712 | 1.000 | 0.080 | 20 | 37758210 | intron variant | G/A | snv | 0.12 | 4 | ||
| rs1340026226 | 1.000 | 0.080 | X | 67711662 | missense variant | G/A | snv | 9.5E-06 | 3 | ||
| rs16986921 | 1.000 | 0.080 | 20 | 37754119 | intron variant | C/T | snv | 0.12 | 3 | ||
| rs141568342 | 1.000 | 0.080 | 22 | 28734532 | missense variant | C/T | snv | 1.6E-04 | 1.5E-04 | 2 | |
| rs266870 | 1.000 | 0.080 | 19 | 50848678 | intron variant | T/C | snv | 0.43 | 2 | ||
| rs10896450 | 1.000 | 0.080 | 11 | 69240647 | regulatory region variant | A/G | snv | 0.55 | 1 | ||
| rs10905371 | 1.000 | 0.080 | 10 | 8438081 | intron variant | A/G | snv | 0.26 | 1 | ||
| rs10905374 | 1.000 | 0.080 | 10 | 8439523 | intron variant | G/A | snv | 0.25 | 1 | ||
| rs10931777 | 1.000 | 0.080 | 2 | 197278867 | intron variant | C/T | snv | 0.72 | 1 | ||
| rs11006207 | 1.000 | 0.080 | 10 | 46057646 | regulatory region variant | A/G | snv | 0.45 | 1 | ||
| rs11135762 | 1.000 | 0.080 | 8 | 23633678 | downstream gene variant | G/A | snv | 0.65 | 1 | ||
| rs111584802 | 1.000 | 0.080 | 5 | 75587055 | missense variant | A/G | snv | 1 | |||
| rs113425597 | 1.000 | 0.080 | 5 | 140807616 | synonymous variant | G/A;C;T | snv | 4.0E-06; 4.4E-03; 4.0E-06 | 1 | ||
| rs114246623 | 1.000 | 0.080 | 3 | 6893379 | intron variant | G/A;C | snv | 4.1E-02 | 1 | ||
| rs114918764 | 1.000 | 0.080 | 4 | 116449550 | intergenic variant | C/T | snv | 2.0E-03 | 1 | ||
| rs115338764 | 1.000 | 0.080 | 5 | 140661602 | non coding transcript exon variant | G/A | snv | 4.4E-03 | 1.8E-02 | 1 | |
| rs11577139 | 1.000 | 0.080 | 1 | 98200569 | intergenic variant | C/A;T | snv | 1 | |||
| rs11988857 | 1.000 | 0.080 | 8 | 127519628 | intergenic variant | G/A | snv | 0.80 | 1 | ||
| rs121908701 | 1.000 | 0.080 | 22 | 28725027 | missense variant | C/T | snv | 1.4E-04 | 6.3E-05 | 1 | |
| rs12537079 | 1.000 | 0.080 | 7 | 118064652 | intergenic variant | T/A;G | snv | 1 | |||
| rs12543663 | 1.000 | 0.080 | 8 | 126912414 | intron variant | C/A;T | snv | 1 | |||
| rs12799883 | 1.000 | 0.080 | 11 | 69243184 | intergenic variant | T/G | snv | 0.51 | 1 | ||
| rs1304454699 | 1.000 | 0.080 | 5 | 75590429 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs13325108 | 1.000 | 0.080 | 3 | 116671823 | intron variant | C/A;G | snv | 1 | |||
| rs137852603 | 1.000 | 0.080 | 10 | 110280017 | missense variant | A/C | snv | 1 |