| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121917834 | 0.790 | 0.080 | 8 | 22163096 | missense variant | T/A;C | snv | 3.6E-05 | 10 | ||
| rs117603931 | 0.882 | 0.080 | 16 | 2319591 | missense variant | C/T | snv | 5.7E-03 | 6.5E-03 | 4 | |
| rs146709251 | 0.882 | 0.080 | 16 | 2279070 | missense variant | G/A | snv | 4.3E-03 | 3.0E-03 | 3 | |
| rs761495176 | 0.882 | 0.080 | 5 | 143400263 | missense variant | T/C | snv | 1.7E-05 | 3 | ||
| rs1042689672 | 0.925 | 0.080 | 10 | 79557504 | missense variant | A/G | snv | 7.0E-06 | 2 | ||
| rs13332514 | 0.925 | 0.080 | 16 | 2317335 | synonymous variant | G/A | snv | 0.17 | 0.12 | 2 | |
| rs17135889 | 0.925 | 0.080 | 16 | 2337259 | intron variant | G/A | snv | 0.11 | 2 | ||
| rs170447 | 1.000 | 0.080 | 16 | 2299370 | intron variant | T/C | snv | 0.51 | 0.45 | 1 | |
| rs1923537 | 1.000 | 0.080 | 10 | 79935452 | intron variant | A/G | snv | 0.37 | 1 | ||
| rs2271255 | 1.000 | 0.080 | 18 | 21044113 | missense variant | T/C | snv | 3.6E-05 | 7.0E-06 | 1 | |
| rs313909 | 1.000 | 0.080 | 16 | 2287992 | intron variant | G/A;C | snv | 0.42; 4.3E-06 | 1 | ||
| rs323043 | 1.000 | 0.080 | 16 | 2298527 | synonymous variant | G/A;C;T | snv | 8.0E-06; 0.14; 4.0E-06 | 1 | ||
| rs370068089 | 1.000 | 0.080 | 8 | 22164041 | stop lost | G/C | snv | 5.6E-05 | 1 | ||
| rs531292167 | 1.000 | 0.080 | 18 | 21006431 | missense variant | T/A | snv | 4.0E-06 | 1 | ||
| rs726843 | 1.000 | 0.080 | 2 | 11216064 | intron variant | G/A | snv | 0.38 | 1 | ||
| rs7956915 | 1.000 | 0.080 | 12 | 6361094 | intron variant | A/G | snv | 0.52 | 1 | ||
| rs952222278 | 1.000 | 0.080 | 7 | 87550238 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs121918563 | 0.827 | 0.120 | 6 | 42721781 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 | 6 | |
| rs1322403577 | 0.882 | 0.120 | 10 | 79613818 | missense variant | T/C | snv | 4.0E-06 | 4 | ||
| rs28451617 | 0.851 | 0.120 | 7 | 99735142 | 5 prime UTR variant | C/T | snv | 9.2E-03 | 3.3E-02 | 4 | |
| rs10178332 | 0.925 | 0.120 | 2 | 11268891 | intron variant | C/A;G | snv | 2 | |||
| rs1130866 | 0.827 | 0.160 | 2 | 85666618 | missense variant | G/A;C | snv | 0.50 | 9 | ||
| rs1966265 | 0.827 | 0.160 | 5 | 177089630 | missense variant | G/A;T | snv | 0.25 | 8 | ||
| rs1124 | 0.882 | 0.160 | 8 | 22164004 | missense variant | G/A | snv | 0.30 | 0.26 | 3 | |
| rs7316 | 0.882 | 0.160 | 2 | 85658890 | 3 prime UTR variant | T/C | snv | 0.14 | 3 |