| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6470494 | 1.000 | 0.080 | 8 | 127075659 | intron variant | T/C | snv | 0.72 | 1 | ||
| rs72725879 | 1.000 | 0.080 | 8 | 127091724 | non coding transcript exon variant | C/T | snv | 0.26 | 1 | ||
| rs59308963 | 1.000 | 0.080 | 2 | 201258757 | intron variant | ATTCTGTC/- | delins | 0.72 | 1 | ||
| rs28441558 | 1.000 | 0.080 | 17 | 7899800 | intron variant | T/C | snv | 4.3E-02 | 1 | ||
| rs4976790 | 1.000 | 0.080 | 5 | 178541914 | intron variant | G/A;C;T | snv | 1 | |||
| rs140659849 | 1.000 | 0.080 | X | 50451939 | intron variant | G/A | snv | 5.6E-03 | 1 | ||
| rs139288166 | 1.000 | 0.080 | 8 | 755922 | intron variant | A/C | snv | 5.9E-03 | 1 | ||
| rs7720298 | 1.000 | 0.080 | 5 | 13858219 | intron variant | C/G | snv | 0.23 | 1 | ||
| rs77581414 | 1.000 | 0.080 | 19 | 10823418 | non coding transcript exon variant | T/A;C | snv | 1 | |||
| rs76551843 | 1.000 | 0.080 | 5 | 169745129 | intron variant | A/G | snv | 5.1E-03 | 1 | ||
| rs1283104 | 1.000 | 0.080 | 3 | 107243674 | intron variant | C/G | snv | 0.43 | 1 | ||
| rs2430386 | 1.000 | 0.080 | 2 | 62950976 | intron variant | C/T | snv | 0.54 | 1 | ||
| rs11290954 | 1.000 | 0.080 | 11 | 76549500 | intron variant | C/- | del | 0.28 | 1 | ||
| rs111599055 | 1.000 | 0.080 | 12 | 132563775 | intron variant | A/C;G | snv | 1 | |||
| rs7295014 | 1.000 | 0.080 | 12 | 132491403 | intron variant | G/A | snv | 0.60 | 1 | ||
| rs139239158 | 1.000 | 0.080 | 3 | 59918603 | intron variant | C/G | snv | 1.4E-02 | 1 | ||
| rs190601686 | 1.000 | 0.080 | 9 | 83585894 | intergenic variant | C/T | snv | 5.1E-03 | 1 | ||
| rs192744896 | 1.000 | 0.080 | 15 | 27501193 | intron variant | T/C | snv | 1.9E-02 | 1 | ||
| rs9306895 | 1.000 | 0.080 | 2 | 20678393 | 3 prime UTR variant | T/C | snv | 0.29 | 1 | ||
| rs17599629 | 1.000 | 0.080 | 1 | 150685811 | intron variant | A/G | snv | 0.17 | 1 | ||
| rs149176864 | 1.000 | 0.080 | 8 | 30701718 | intron variant | G/A | snv | 2.1E-02 | 1 | ||
| rs1048169 | 1.000 | 0.080 | 9 | 19055967 | 3 prime UTR variant | T/C | snv | 0.46 | 1 | ||
| rs11214775 | 1.000 | 0.080 | 11 | 113936459 | intron variant | G/A | snv | 0.29 | 1 | ||
| rs2277283 | 1.000 | 0.080 | 11 | 62140968 | missense variant | T/A;C | snv | 0.24 | 0.25 | 1 | |
| rs11574532 | 1.000 | 0.080 | 12 | 53200654 | intron variant | C/T | snv | 7.3E-02 | 1 |