| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9263739 | 1.000 | 0.040 | 6 | 31143579 | intron variant | C/T | snv | 0.16 | 1 | ||
| rs12261843 | 1.000 | 0.040 | 10 | 35265126 | intron variant | T/C;G | snv | 1 | |||
| rs6499188 | 1.000 | 0.040 | 16 | 68640885 | intron variant | G/A;C | snv | 1 | |||
| rs10415946 | 1.000 | 0.040 | 19 | 41755151 | intron variant | A/G | snv | 0.39 | 1 | ||
| rs28374715 | 1.000 | 0.040 | 15 | 41271752 | intron variant | A/G | snv | 0.25 | 1 | ||
| rs1336123245 | 1.000 | 0.040 | 1 | 74710189 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs17736589 | 1.000 | 0.040 | 17 | 78741036 | intron variant | A/G | snv | 0.15 | 1 | ||
| rs267939 | 1.000 | 0.040 | 5 | 10752203 | intron variant | C/T | snv | 0.50 | 1 | ||
| rs11583043 | 1.000 | 0.040 | 1 | 101000498 | intron variant | C/T | snv | 0.28 | 1 | ||
| rs11054935 | 1.000 | 0.040 | 12 | 12495909 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs4905 | 1.000 | 0.040 | 19 | 4237070 | synonymous variant | A/G | snv | 0.34 | 0.40 | 1 | |
| rs10035653 | 1.000 | 0.040 | 5 | 442675 | non coding transcript exon variant | G/A;T | snv | 9.1E-02; 4.0E-06 | 1 | ||
| rs511278 | 1.000 | 0.040 | 1 | 161521106 | intron variant | T/A;C | snv | 1 | |||
| rs76901167 | 1.000 | 0.040 | 6 | 32608701 | regulatory region variant | T/A;C | snv | 1 | |||
| rs9269955 | 1.000 | 0.040 | 6 | 32584361 | missense variant | G/A;C;T | snv | 4.7E-05; 5.9E-03 | 1 | ||
| rs2870946 | 1.000 | 0.040 | 12 | 68202881 | intron variant | T/C | snv | 7.0E-02 | 1 | ||
| rs7134472 | 1.000 | 0.040 | 12 | 68106206 | intron variant | G/A | snv | 0.32 | 1 | ||
| rs2228054 | 1.000 | 0.040 | 11 | 117993398 | synonymous variant | G/A | snv | 8.3E-02 | 5.0E-02 | 1 | |
| rs713669 | 1.000 | 0.040 | 22 | 50013342 | upstream gene variant | C/G;T | snv | 1 | |||
| rs880790 | 1.000 | 0.040 | 1 | 206786871 | intron variant | C/T | snv | 0.68 | 1 | ||
| rs6543115 | 1.000 | 0.040 | 2 | 102311181 | upstream gene variant | C/A;G | snv | 1 | |||
| rs2232360 | 1.000 | 0.040 | 1 | 206867314 | intron variant | G/A;C | snv | 1 | |||
| rs7591368 | 1.000 | 0.040 | 2 | 15722206 | intron variant | C/A | snv | 0.43 | 1 | ||
| rs113986290 | 1.000 | 0.040 | 6 | 19780778 | intron variant | C/G;T | snv | 1 | |||
| rs10910092 | 1.000 | 0.040 | 1 | 2570077 | downstream gene variant | A/G | snv | 0.52 | 1 |