| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2075559 | 0.882 | 0.040 | 17 | 50189930 | intron variant | G/A;C;T | snv | 0.52; 4.0E-06 | 3 | ||
| rs2236947 | 0.882 | 0.040 | 3 | 50334001 | intron variant | C/A | snv | 0.39 | 3 | ||
| rs231755 | 0.882 | 0.040 | 2 | 203888846 | regulatory region variant | G/C | snv | 0.11 | 3 | ||
| rs235764 | 0.882 | 0.040 | 20 | 6773599 | intron variant | G/A | snv | 0.31 | 3 | ||
| rs29001322 | 0.882 | 0.040 | 10 | 97462918 | non coding transcript exon variant | A/C;G | snv | 3 | |||
| rs3787547 | 0.882 | 0.040 | 20 | 54067899 | intron variant | G/A | snv | 0.36 | 3 | ||
| rs4148416 | 0.882 | 0.040 | 17 | 50676062 | synonymous variant | C/T | snv | 8.7E-02 | 0.10 | 3 | |
| rs454006 | 0.882 | 0.040 | 19 | 53886867 | intron variant | T/C | snv | 0.36 | 3 | ||
| rs58834075 | 0.882 | 0.040 | 14 | 101066756 | non coding transcript exon variant | C/G;T | snv | 4.0E-06; 4.6E-02 | 3 | ||
| rs756673959 | 0.882 | 0.040 | 12 | 68828867 | stop lost | T/G | snv | 3 | |||
| rs758300152 | 0.882 | 0.040 | 14 | 44504889 | missense variant | T/C;G | snv | 1.6E-05; 4.0E-06 | 3 | ||
| rs7591996 | 0.882 | 0.040 | 2 | 6321289 | intron variant | A/C | snv | 0.57 | 3 | ||
| rs764191858 | 0.882 | 0.040 | 4 | 185502359 | missense variant | G/A | snv | 3 | |||
| rs770771727 | 0.882 | 0.040 | 6 | 144751941 | missense variant | A/C;G | snv | 4.5E-05; 2.5E-05 | 3 | ||
| rs779591039 | 0.882 | 0.040 | 20 | 45253712 | missense variant | G/A | snv | 3 | |||
| rs780673045 | 0.882 | 0.040 | 12 | 68839592 | missense variant | A/G | snv | 1.2E-05 | 3 | ||
| rs8103992 | 0.882 | 0.040 | 19 | 19554834 | regulatory region variant | A/C;T | snv | 3 | |||
| rs9866361 | 0.882 | 0.040 | 3 | 179190061 | intron variant | G/A | snv | 0.24 | 3 | ||
| rs998074 | 0.882 | 0.040 | 6 | 160047351 | intron variant | T/A;C | snv | 0.53 | 3 | ||
| rs998075 | 0.882 | 0.040 | 6 | 160047246 | synonymous variant | A/G | snv | 0.53 | 0.54 | 3 | |
| rs2070699 | 0.752 | 0.080 | 6 | 12292539 | intron variant | G/C;T | snv | 0.45 | 14 | ||
| rs367597251 | 0.807 | 0.080 | 12 | 68839587 | missense variant | A/G | snv | 1.5E-04 | 5.1E-04 | 10 | |
| rs12894467 | 0.807 | 0.080 | 14 | 101041390 | non coding transcript exon variant | C/T | snv | 0.51 | 0.50 | 6 | |
| rs171140 | 0.807 | 0.080 | 19 | 45361744 | non coding transcript exon variant | C/A | snv | 0.58 | 0.64 | 6 | |
| rs3745406 | 0.851 | 0.080 | 19 | 53891711 | missense variant | T/A;C | snv | 4.0E-06; 0.41 | 6 |