Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10020432 | 0.925 | 0.080 | 4 | 73455883 | 3 prime UTR variant | A/G | snv | 0.54 | 2 | ||
rs10053538 | 0.807 | 0.160 | 5 | 157110499 | intron variant | C/A;T | snv | 7 | |||
rs1012068 | 0.827 | 0.160 | 22 | 31869917 | intron variant | T/G | snv | 0.37 | 5 | ||
rs10146249 | 1.000 | 0.080 | 14 | 92074996 | intron variant | C/A | snv | 0.29 | 1 | ||
rs10204525 | 0.701 | 0.440 | 2 | 241850169 | 3 prime UTR variant | C/T | snv | 0.21 | 20 | ||
rs1041740 | 0.807 | 0.320 | 21 | 31667849 | intron variant | C/T | snv | 0.24 | 8 | ||
rs10433937 | 0.882 | 0.080 | 4 | 87308948 | intron variant | T/A;C;G | snv | 4 | |||
rs1049305 | 0.925 | 0.160 | 7 | 30924207 | 3 prime UTR variant | G/C | snv | 0.52 | 4 | ||
rs1054690270 | 0.827 | 0.160 | 8 | 144505907 | frameshift variant | CT/- | delins | 5 | |||
rs1056836 | 0.581 | 0.680 | 2 | 38071060 | missense variant | G/C | snv | 0.51 | 58 | ||
rs1059122 | 0.882 | 0.160 | 4 | 88726273 | 3 prime UTR variant | T/A | snv | 0.46 | 3 | ||
rs10932029 | 0.827 | 0.200 | 2 | 203937045 | intron variant | T/A;C | snv | 5 | |||
rs10945859 | 0.882 | 0.120 | 6 | 162721570 | intron variant | T/C | snv | 0.17 | 3 | ||
rs11003123 | 0.827 | 0.200 | 10 | 52771774 | upstream gene variant | G/A | snv | 0.30 | 6 | ||
rs1127354 | 0.667 | 0.400 | 20 | 3213196 | missense variant | C/A;G | snv | 7.5E-02 | 26 | ||
rs1140409 | 0.925 | 0.080 | 17 | 64500552 | missense variant | A/C | snv | 5.4E-02 | 5.0E-02 | 2 | |
rs11554495 | 0.701 | 0.240 | 12 | 52904798 | missense variant | C/A | snv | 4.9E-03 | 5.4E-03 | 19 | |
rs1161457931 | 0.763 | 0.200 | 22 | 37084836 | missense variant | C/T | snv | 6.4E-06 | 9 | ||
rs11614913 | 0.512 | 0.760 | 12 | 53991815 | mature miRNA variant | C/T | snv | 0.39 | 0.34 | 111 | |
rs11977021 | 0.827 | 0.240 | 7 | 106288069 | upstream gene variant | C/T | snv | 0.22 | 5 | ||
rs1201810520 | 0.925 | 0.160 | 2 | 88590497 | missense variant | C/T | snv | 2 | |||
rs12075 | 0.724 | 0.240 | 1 | 159205564 | missense variant | G/A | snv | 0.51 | 0.66 | 22 | |
rs1208663703 | 0.763 | 0.200 | 22 | 37086414 | missense variant | T/C | snv | 5.2E-06 | 7.0E-06 | 9 | |
rs12104272 | 0.925 | 0.080 | 19 | 49644795 | intron variant | G/A | snv | 0.44 | 2 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 |