| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1010273 | 0.882 | 0.120 | 6 | 106107150 | synonymous variant | G/A | snv | 9.7E-02 | 7.7E-02 | 3 | |
| rs548234 | 0.763 | 0.360 | 6 | 106120159 | intron variant | C/T | snv | 0.76 | 11 | ||
| rs6568431 | 0.790 | 0.320 | 6 | 106140931 | intron variant | A/C | snv | 0.61 | 7 | ||
| rs61330082 | 0.732 | 0.320 | 7 | 106286419 | upstream gene variant | G/A | snv | 0.22 | 13 | ||
| rs11977021 | 0.827 | 0.240 | 7 | 106288069 | upstream gene variant | C/T | snv | 0.22 | 5 | ||
| rs510432 | 0.752 | 0.280 | 6 | 106326155 | upstream gene variant | T/C | snv | 0.57 | 11 | ||
| rs17067724 | 1.000 | 0.080 | 6 | 106786391 | intron variant | A/G | snv | 5.2E-03 | 1 | ||
| rs1305420126 | 1.000 | 0.080 | 4 | 106924184 | synonymous variant | G/A | snv | 8.0E-06 | 1 | ||
| rs3809236 | 1.000 | 0.080 | 12 | 107093269 | 5 prime UTR variant | G/A;C | snv | 0.14 | 1 | ||
| rs7442180 | 1.000 | 0.080 | 4 | 107956127 | intron variant | C/A | snv | 1 | |||
| rs221330 | 1.000 | 0.080 | 4 | 108000211 | intron variant | G/A | snv | 0.24 | 1 | ||
| rs74723057 | 1.000 | 0.080 | 19 | 10818611 | intron variant | G/C | snv | 6.0E-02 | 1 | ||
| rs1469557 | 0.925 | 0.120 | 8 | 10849291 | downstream gene variant | C/T | snv | 0.18 | 2 | ||
| rs3890995 | 1.000 | 0.080 | 12 | 109095724 | upstream gene variant | T/C | snv | 0.19 | 1 | ||
| rs1049112 | 1.000 | 0.080 | 12 | 10930757 | missense variant | A/G;T | snv | 0.11; 1.4E-05 | 1 | ||
| rs11879293 | 0.882 | 0.120 | 19 | 10961934 | intron variant | G/A;C;T | snv | 4 | |||
| rs4444903 | 0.630 | 0.360 | 4 | 109912954 | 5 prime UTR variant | A/G | snv | 0.51 | 35 | ||
| rs1336242054 | 1.000 | 0.080 | 4 | 109974747 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs11569017 | 0.925 | 0.120 | 4 | 109980955 | missense variant | A/T | snv | 7.3E-02 | 5.0E-02 | 2 | |
| rs12711521 | 0.807 | 0.240 | 1 | 11030859 | missense variant | C/A | snv | 0.74 | 0.63 | 7 | |
| rs72550870 | 0.776 | 0.360 | 1 | 11046609 | missense variant | T/C | snv | 2.1E-02 | 2.2E-02 | 8 | |
| rs4938723 | 0.574 | 0.680 | 11 | 111511840 | intron variant | T/C | snv | 0.32 | 60 | ||
| rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
| rs10789859 | 1.000 | 0.080 | 11 | 112089809 | intron variant | T/C | snv | 0.31 | 1 | ||
| rs187238 | 0.602 | 0.680 | 11 | 112164265 | intron variant | C/A;G | snv | 48 |