| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2516513 | 0.925 | 0.120 | 6 | 31479811 | downstream gene variant | C/T | snv | 0.20 | 5 | ||
| rs1860661 | 0.882 | 0.120 | 19 | 1650135 | intron variant | A/C;G | snv | 6.7E-06; 0.54 | 3 | ||
| rs3781093 | 0.882 | 0.120 | 10 | 8059964 | intron variant | T/C | snv | 0.19 | 3 | ||
| rs649775 | 0.882 | 0.120 | 6 | 33716536 | upstream gene variant | A/G;T | snv | 3 | |||
| rs13255292 | 0.925 | 0.120 | 8 | 128064327 | intron variant | C/T | snv | 0.24 | 2 | ||
| rs34972832 | 0.925 | 0.120 | 16 | 11105081 | intron variant | G/A;T | snv | 0.14 | 2 | ||
| rs6928977 | 0.925 | 0.120 | 6 | 135305210 | intron variant | T/G | snv | 0.70 | 2 | ||
| rs7745098 | 1.000 | 0.120 | 6 | 135093866 | intron variant | C/G;T | snv | 2 | |||
| rs1002658 | 1.000 | 0.120 | 6 | 137660447 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs1244186 | 1.000 | 0.120 | 10 | 8050720 | non coding transcript exon variant | T/A;C | snv | 1 | |||
| rs1432295 | 1.000 | 0.120 | 2 | 60839531 | intron variant | G/A | snv | 0.69 | 1 | ||
| rs2069757 | 1.000 | 0.120 | 5 | 132662721 | intron variant | G/A | snv | 7.5E-02 | 1 | ||
| rs2240064 | 1.000 | 0.120 | 6 | 31146796 | intron variant | G/A;T | snv | 1 | |||
| rs2523710 | 1.000 | 0.120 | 6 | 31483132 | intron variant | G/A | snv | 0.14 | 1 | ||
| rs2608053 | 1.000 | 0.120 | 8 | 128063586 | intron variant | T/C | snv | 0.50 | 1 | ||
| rs2855430 | 1.000 | 0.120 | 6 | 33173503 | missense variant | G/A | snv | 0.12 | 9.9E-02 | 1 | |
| rs3093998 | 1.000 | 0.120 | 6 | 31517397 | downstream gene variant | C/A | snv | 0.70 | 1 | ||
| rs3130237 | 1.000 | 0.120 | 6 | 33129784 | downstream gene variant | T/C | snv | 0.13 | 1 | ||
| rs387906223 | 1.000 | 0.120 | 3 | 49171662 | 5 prime UTR variant | C/T | snv | 4.8E-03 | 1 | ||
| rs4733809 | 1.000 | 0.120 | 8 | 127977046 | intron variant | C/T | snv | 0.54 | 1 | ||
| rs485411 | 1.000 | 0.120 | 10 | 8051222 | non coding transcript exon variant | T/A;C;G | snv | 0.81 | 1 | ||
| rs501764 | 1.000 | 0.120 | 10 | 8051071 | non coding transcript exon variant | G/T | snv | 0.87 | 0.86 | 1 | |
| rs6439924 | 1.000 | 0.120 | 3 | 140450815 | intron variant | A/C | snv | 0.21 | 1 | ||
| rs6565176 | 1.000 | 0.120 | 16 | 30163605 | intergenic variant | T/A;C | snv | 1 | |||
| rs7111520 | 1.000 | 0.120 | 11 | 111378886 | intron variant | G/A | snv | 0.58 | 1 |