Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10010131 | 0.827 | 0.120 | 4 | 6291188 | intron variant | A/G | snv | 0.66 | 0.63 | 7 | |
rs1058046 | 0.925 | 0.120 | 17 | 43953163 | missense variant | G/C | snv | 0.63 | 0.59 | 2 | |
rs10885406 | 0.925 | 0.120 | 10 | 113017965 | intron variant | A/G | snv | 0.55 | 2 | ||
rs10968576 | 0.882 | 0.120 | 9 | 28414341 | intron variant | A/G | snv | 0.26 | 10 | ||
rs11075989 | 0.925 | 0.120 | 16 | 53785965 | intron variant | C/A;T | snv | 3 | |||
rs11075990 | 0.925 | 0.120 | 16 | 53785981 | intron variant | A/G | snv | 0.41 | 6 | ||
rs11076023 | 0.925 | 0.120 | 16 | 54118136 | 3 prime UTR variant | A/T | snv | 0.49 | 2 | ||
rs11642015 | 0.925 | 0.120 | 16 | 53768582 | intron variant | C/T | snv | 0.31 | 9 | ||
rs11642841 | 0.925 | 0.120 | 16 | 53811575 | intron variant | C/A;G | snv | 3 | |||
rs116454156 | 0.925 | 0.120 | 10 | 93587284 | missense variant | G/A | snv | 1.8E-02 | 1.4E-02 | 3 | |
rs11671664 | 0.925 | 0.120 | 19 | 45669020 | intron variant | G/A | snv | 0.12 | 5 | ||
rs11960429 | 0.925 | 0.120 | 5 | 180739677 | missense variant | G/A | snv | 1.2E-02 | 1.5E-02 | 2 | |
rs12104705 | 0.882 | 0.120 | 2 | 162435107 | intron variant | C/T | snv | 0.15 | 4 | ||
rs12156368 | 0.925 | 0.120 | 8 | 18885203 | intron variant | C/T | snv | 0.36 | 2 | ||
rs13078807 | 0.925 | 0.120 | 3 | 85835000 | intron variant | A/G | snv | 0.15 | 5 | ||
rs1412239 | 0.925 | 0.120 | 9 | 28425517 | intron variant | C/G | snv | 0.26 | 4 | ||
rs150016118 | 0.882 | 0.120 | 11 | 74006339 | missense variant | A/G | snv | 1.7E-05 | 6.3E-05 | 6 | |
rs1541276 | 0.925 | 0.120 | 18 | 13825728 | splice region variant | A/C | snv | 0.17 | 0.19 | 2 | |
rs1550805 | 0.925 | 0.120 | 5 | 68287979 | intron variant | C/T | snv | 6.9E-02 | 2 | ||
rs1558902 | 0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 | 21 | ||
rs16861194 | 0.925 | 0.120 | 3 | 186841636 | upstream gene variant | A/G | snv | 0.15 | 2 | ||
rs17700633 | 0.882 | 0.120 | 18 | 60262199 | intergenic variant | G/A | snv | 0.28 | 4 | ||
rs17817964 | 0.925 | 0.120 | 16 | 53794154 | intron variant | C/T | snv | 0.30 | 6 | ||
rs1797 | 0.925 | 0.120 | 10 | 117945927 | intergenic variant | C/T | snv | 0.45 | 2 | ||
rs1805081 | 0.925 | 0.120 | 18 | 23560468 | missense variant | T/C | snv | 0.33 | 0.29 | 3 |