| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs763222239 | 0.827 | 0.040 | 3 | 184322862 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
| rs1801334 | 0.851 | 0.040 | 6 | 161360193 | missense variant | C/T | snv | 2.5E-02 | 2.5E-02 | 4 | |
| rs34410987 | 0.882 | 0.040 | 12 | 40283897 | missense variant | C/T | snv | 7.4E-04 | 2.2E-04 | 3 | |
| rs752169833 | 0.925 | 0.040 | 7 | 56102878 | missense variant | C/A;T | snv | 8.0E-06; 5.6E-05 | 3 | ||
| rs947211 | 0.925 | 0.040 | 1 | 205783537 | non coding transcript exon variant | A/G | snv | 0.64 | 3 | ||
| rs10746953 | 0.925 | 0.040 | 9 | 74302924 | regulatory region variant | C/T | snv | 0.44 | 2 | ||
| rs10788972 | 0.925 | 0.040 | 1 | 54106570 | intron variant | C/A | snv | 0.57 | 2 | ||
| rs11186 | 0.925 | 0.040 | 2 | 189032668 | 3 prime UTR variant | A/C | snv | 9.4E-02 | 2 | ||
| rs13153459 | 0.925 | 0.040 | 5 | 44515833 | intron variant | A/C;T | snv | 2 | |||
| rs1362858 | 0.925 | 0.040 | 18 | 35406636 | upstream gene variant | C/A | snv | 0.71 | 2 | ||
| rs1366901063 | 0.925 | 0.040 | 11 | 123060725 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs1559085 | 0.925 | 0.040 | 5 | 96742998 | intron variant | A/G | snv | 9.4E-02 | 2 | ||
| rs1879553 | 0.925 | 0.040 | 3 | 118896616 | downstream gene variant | A/G | snv | 7.3E-02 | 2 | ||
| rs374880482 | 0.925 | 0.040 | X | 85963748 | missense variant | T/C | snv | 3.3E-05 | 2.8E-05 | 2 | |
| rs56285021 | 0.925 | 0.040 | 5 | 122422868 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs66737902 | 0.925 | 0.040 | 12 | 40367861 | 3 prime UTR variant | T/C | snv | 0.14 | 2 | ||
| rs6783485 | 0.925 | 0.040 | 3 | 59442071 | intron variant | G/A | snv | 5.1E-02 | 2 | ||
| rs7669 | 0.925 | 0.040 | 13 | 27435714 | missense variant | G/A;C | snv | 0.15 | 0.15 | 2 | |
| rs7702187 | 0.925 | 0.040 | 5 | 9332169 | intron variant | T/A | snv | 0.70 | 2 | ||
| rs823144 | 0.925 | 0.040 | 1 | 205775418 | 5 prime UTR variant | C/A;G | snv | 2 | |||
| rs849898 | 0.925 | 0.040 | 1 | 227966216 | intergenic variant | A/C;G | snv | 2 | |||
| rs9323124 | 0.925 | 0.040 | 14 | 46996974 | non coding transcript exon variant | T/A | snv | 0.23 | 2 | ||
| rs12046178 | 1.000 | 0.040 | 1 | 54106502 | intron variant | T/C | snv | 0.30 | 1 | ||
| rs1320254777 | 1.000 | 0.040 | 14 | 54902565 | missense variant | G/C | snv | 7.0E-06 | 1 | ||
| rs27852 | 1.000 | 0.040 | 5 | 96710335 | intron variant | A/C;G | snv | 1 |