| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057941 | 0.701 | 0.280 | 1 | 155216951 | non coding transcript exon variant | G/A;T | snv | 0.46 | 18 | ||
| rs11119608 | 0.708 | 0.280 | 1 | 210816167 | intron variant | T/G | snv | 0.21 | 17 | ||
| rs186507655 | 0.708 | 0.280 | 1 | 1351675 | upstream gene variant | G/A | snv | 6.8E-03 | 17 | ||
| rs2974935 | 0.708 | 0.280 | 1 | 155212052 | non coding transcript exon variant | G/A;C;T | snv | 17 | |||
| rs34517439 | 0.882 | 0.120 | 1 | 77984833 | intron variant | C/A | snv | 7.3E-02 | 7 | ||
| rs17391694 | 0.882 | 0.120 | 1 | 78157942 | regulatory region variant | C/T | snv | 7.8E-02 | 5 | ||
| rs4072037 | 0.732 | 0.240 | 1 | 155192276 | splice acceptor variant | C/A;T | snv | 0.59 | 4 | ||
| rs71658797 | 0.925 | 0.080 | 1 | 77501822 | intron variant | T/A | snv | 7.3E-02 | 3 | ||
| rs35535570 | 1.000 | 0.040 | 1 | 77794071 | intron variant | G/A | snv | 5.2E-02 | 1 | ||
| rs3827760 | 0.752 | 0.160 | 2 | 108897145 | missense variant | A/G | snv | 0.15 | 5.9E-02 | 6 | |
| rs79294676 | 0.925 | 0.080 | 2 | 67277529 | intron variant | G/A | snv | 6.4E-03 | 2 | ||
| rs114928225 | 1.000 | 0.040 | 2 | 118692164 | intergenic variant | T/A | snv | 1.0E-02 | 1 | ||
| rs148944993 | 1.000 | 0.040 | 2 | 234452501 | intron variant | G/A | snv | 2.0E-03 | 1 | ||
| rs17038564 | 1.000 | 0.040 | 2 | 65268924 | 3 prime UTR variant | A/G | snv | 5.3E-02 | 1 | ||
| rs191524990 | 1.000 | 0.040 | 2 | 68069083 | intron variant | A/T | snv | 7.6E-03 | 1 | ||
| rs59396197 | 1.000 | 0.040 | 2 | 139675756 | intergenic variant | G/A | snv | 9.1E-02 | 1 | ||
| rs481519 | 0.708 | 0.280 | 3 | 27285723 | intron variant | C/A;T | snv | 17 | |||
| rs75316749 | 0.701 | 0.280 | 3 | 169043635 | intergenic variant | A/G | snv | 4.2E-02 | 17 | ||
| rs11375254 | 0.882 | 0.080 | 3 | 189625454 | intergenic variant | A/-;AA;AAA;AAAA | delins | 3 | |||
| rs13080835 | 0.925 | 0.080 | 3 | 189639410 | intron variant | G/T | snv | 0.45 | 2 | ||
| rs2293607 | 0.807 | 0.200 | 3 | 169764547 | non coding transcript exon variant | T/A;C | snv | 2 | |||
| rs10937405 | 0.807 | 0.080 | 3 | 189665394 | intron variant | C/T | snv | 0.38 | 1 | ||
| rs114807680 | 1.000 | 0.040 | 3 | 135085649 | intron variant | G/A | snv | 9.8E-03 | 1 | ||
| rs13314271 | 0.925 | 0.080 | 3 | 189639813 | intron variant | T/C | snv | 0.45 | 1 | ||
| rs2131877 | 0.827 | 0.080 | 3 | 195137645 | intron variant | G/A | snv | 0.20 | 1 |