| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2235751 | 0.882 | 0.120 | 20 | 1989288 | intron variant | A/G | snv | 0.40 | 3 | ||
| rs63751399 | 0.882 | 0.120 | 14 | 73171047 | missense variant | T/A;C | snv | 3 | |||
| rs142690225 | 0.925 | 0.080 | 1 | 226894111 | missense variant | G/A | snv | 1.1E-04 | 1.1E-04 | 3 | |
| rs4879809 | 0.882 | 0.120 | 9 | 34635601 | 3 prime UTR variant | T/A;C;G | snv | 1.1E-03; 1.00 | 3 | ||
| rs1043202 | 0.882 | 0.080 | 12 | 54182178 | missense variant | T/A | snv | 3 | |||
| rs1010159 | 0.882 | 0.080 | 11 | 121612692 | non coding transcript exon variant | C/T | snv | 0.55 | 0.55 | 3 | |
| rs2618516 | 0.882 | 0.080 | 11 | 14000092 | intron variant | T/C | snv | 0.65 | 3 | ||
| rs766647311 | 0.882 | 0.080 | 6 | 41159841 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
| rs1401663578 | 0.882 | 0.120 | 17 | 63483037 | missense variant | A/G | snv | 1.4E-05 | 4 | ||
| rs1233347077 | 0.851 | 0.160 | 19 | 44905894 | missense variant | G/C | snv | 7.0E-06 | 4 | ||
| rs763872192 | 0.882 | 0.080 | 7 | 80672000 | missense variant | C/T | snv | 2.8E-05 | 4 | ||
| rs223330 | 0.851 | 0.160 | 4 | 102872502 | intron variant | T/A;C | snv | 4 | |||
| rs9331896 | 0.851 | 0.080 | 8 | 27610169 | intron variant | C/G;T | snv | 4 | |||
| rs773819452 | 0.851 | 0.200 | 10 | 73160449 | missense variant | G/A | snv | 4.2E-06 | 4 | ||
| rs763841075 | 0.851 | 0.120 | 17 | 44350293 | missense variant | T/C | snv | 1.8E-04 | 1.1E-04 | 4 | |
| rs9357347 | 0.851 | 0.080 | 6 | 41182853 | intergenic variant | A/C;T | snv | 4 | |||
| rs63751011 | 0.925 | 0.120 | 17 | 46010418 | intron variant | C/T | snv | 4 | |||
| rs6332 | 0.851 | 0.080 | 12 | 5494466 | synonymous variant | G/A;T | snv | 0.49; 3.2E-05 | 4 | ||
| rs1997794 | 0.851 | 0.120 | 20 | 1994212 | 5 prime UTR variant | T/C | snv | 0.50 | 4 | ||
| rs910080 | 0.851 | 0.120 | 20 | 1979580 | 3 prime UTR variant | A/G | snv | 0.35 | 4 | ||
| rs2281983 | 0.851 | 0.080 | 10 | 102231624 | missense variant | G/A;C;T | snv | 0.62; 8.3E-06 | 4 | ||
| rs1801474 | 0.851 | 0.080 | 6 | 162201165 | missense variant | C/T | snv | 7.1E-02 | 5.3E-02 | 4 | |
| rs571825723 | 0.925 | 0.080 | 14 | 73211867 | missense variant | C/T | snv | 4.4E-05 | 2.8E-05 | 4 | |
| rs63750004 | 0.851 | 0.080 | 14 | 73173655 | missense variant | T/A;C | snv | 4 | |||
| rs6347 | 0.851 | 0.080 | 5 | 1411297 | synonymous variant | T/C | snv | 0.23 | 0.32 | 4 |