Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs2234767 | 0.649 | 0.280 | 10 | 88989499 | intron variant | G/A;T | snv | 0.15 | 30 | ||
rs11568820 | 0.672 | 0.480 | 12 | 47908762 | intron variant | C/T | snv | 0.38 | 27 | ||
rs72928038 | 0.695 | 0.360 | 6 | 90267049 | intron variant | G/A | snv | 0.11 | 19 | ||
rs4409785 | 0.752 | 0.240 | 11 | 95578258 | intron variant | T/C | snv | 0.13 | 12 | ||
rs121434257 | 0.827 | 0.080 | 21 | 44289686 | missense variant | G/A;T | snv | 4.0E-05 | 6 | ||
rs1534422 | 0.827 | 0.160 | 2 | 12500615 | intron variant | G/A | snv | 0.52 | 6 | ||
rs2270450 | 0.827 | 0.200 | 6 | 46677138 | 3 prime UTR variant | C/T | snv | 0.29 | 5 | ||
rs706779 | 0.827 | 0.160 | 10 | 6056861 | intron variant | T/C | snv | 0.48 | 5 | ||
rs13093110 | 0.882 | 0.120 | 3 | 188407332 | intron variant | C/T | snv | 0.42 | 4 | ||
rs17759659 | 0.851 | 0.120 | 18 | 63291411 | intron variant | A/G | snv | 0.31 | 4 | ||
rs11571297 | 0.882 | 0.120 | 2 | 203880280 | regulatory region variant | T/C | snv | 0.44 | 3 | ||
rs57348955 | 0.882 | 0.120 | 16 | 31174561 | upstream gene variant | G/A;C | snv | 3 | |||
rs7537605 | 0.882 | 0.120 | 1 | 107800465 | intron variant | G/A;T | snv | 3 | |||
rs1133076 | 0.925 | 0.080 | 8 | 133113438 | missense variant | G/A | snv | 0.48 | 0.56 | 2 |