Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs76418789 | 0.882 | 0.080 | 1 | 67182913 | missense variant | G/A | snv | 7.3E-03 | 4.5E-03 | 2 | |
rs35018800 | 0.790 | 0.160 | 19 | 10354167 | missense variant | G/A | snv | 4.6E-03 | 4.9E-03 | 5 | |
rs141992399 | 0.827 | 0.120 | 9 | 136365140 | splice donor variant | C/G;T | snv | 3.3E-03; 4.0E-06 | 5 | ||
rs148783236 | 1.000 | 0.040 | 15 | 50492819 | missense variant | A/C;G | snv | 2.5E-03 | 1 | ||
rs61752717 | 0.583 | 0.840 | 16 | 3243407 | missense variant | T/A;C | snv | 2.8E-04 | 1 | ||
rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 25 | ||
rs72928038 | 0.695 | 0.360 | 6 | 90267049 | intron variant | G/A | snv | 0.11 | 19 | ||
rs4625 | 0.716 | 0.280 | 3 | 49534707 | 3 prime UTR variant | A/G | snv | 0.30 | 17 | ||
rs4676410 | 0.716 | 0.240 | 2 | 240624322 | intron variant | G/A | snv | 0.26 | 17 | ||
rs1689510 | 0.724 | 0.240 | 12 | 56002984 | non coding transcript exon variant | G/C | snv | 0.25 | 16 | ||
rs12232497 | 0.701 | 0.360 | 17 | 39883866 | intergenic variant | T/C | snv | 0.35 | 15 | ||
rs12598357 | 0.724 | 0.240 | 16 | 28329624 | intergenic variant | A/G | snv | 0.43 | 15 | ||
rs2836882 | 0.724 | 0.240 | 21 | 39094644 | intergenic variant | G/A | snv | 0.23 | 15 | ||
rs36051895 | 0.716 | 0.240 | 9 | 4981866 | upstream gene variant | G/T | snv | 0.25 | 15 | ||
rs62324212 | 0.724 | 0.240 | 4 | 122639784 | intron variant | C/A;G | snv | 15 | |||
rs706778 | 0.695 | 0.320 | 10 | 6056986 | intron variant | C/T | snv | 0.46 | 15 | ||
rs7725052 | 0.716 | 0.240 | 5 | 40487168 | intron variant | C/T | snv | 0.52 | 15 | ||
rs7731626 | 0.716 | 0.240 | 5 | 56148856 | intron variant | G/A | snv | 0.30 | 15 | ||
rs10822050 | 0.724 | 0.240 | 10 | 62679011 | downstream gene variant | T/C | snv | 0.33 | 14 | ||
rs10988542 | 0.724 | 0.240 | 9 | 129894985 | intron variant | G/A;C | snv | 14 | |||
rs11145763 | 0.724 | 0.240 | 9 | 136369144 | intron variant | A/C;G;T | snv | 14 | |||
rs114846446 | 0.724 | 0.240 | 2 | 2944140 | intron variant | G/A | snv | 9.5E-03 | 14 | ||
rs11580078 | 0.724 | 0.240 | 1 | 67203951 | intron variant | C/A;G | snv | 14 | |||
rs117372389 | 0.724 | 0.240 | 16 | 50634166 | 3 prime UTR variant | G/T | snv | 1.1E-02 | 14 | ||
rs11741255 | 0.724 | 0.240 | 5 | 132475490 | intron variant | G/A | snv | 0.29 | 14 |