Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs579459 | 0.752 | 0.320 | 9 | 133278724 | upstream gene variant | C/T | snv | 0.81 | 17 | ||
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 17 | ||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 14 | |
rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 11 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 10 | |
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 10 | ||
rs2736100 | 0.550 | 0.880 | 5 | 1286401 | 3 prime UTR variant | C/A | snv | 0.52 | 9 | ||
rs4820268 | 0.851 | 0.160 | 22 | 37073551 | missense variant | G/A;C | snv | 0.53; 4.0E-06 | 9 | ||
rs495828 | 0.827 | 0.200 | 9 | 133279294 | upstream gene variant | T/G | snv | 0.81 | 8 | ||
rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 8 | ||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 8 | ||
rs9494145 | 0.925 | 0.080 | 6 | 135111414 | intergenic variant | T/A;C | snv | 7 | |||
rs129128 | 6 | 26125114 | intron variant | C/T | snv | 0.91 | 7 | ||||
rs4895441 | 0.925 | 0.080 | 6 | 135105435 | upstream gene variant | A/G | snv | 0.21 | 7 | ||
rs12216125 | 0.925 | 0.120 | 6 | 25997230 | intron variant | C/T | snv | 0.26 | 6 | ||
rs130624 | 22 | 37042611 | regulatory region variant | G/T | snv | 0.47 | 6 | ||||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 6 | ||
rs9399137 | 0.851 | 0.320 | 6 | 135097880 | intron variant | T/C | snv | 0.20 | 6 | ||
rs9376092 | 0.851 | 0.120 | 6 | 135106006 | upstream gene variant | C/A | snv | 0.24 | 6 | ||
rs228129 | 22 | 37032558 | upstream gene variant | A/G | snv | 0.48 | 6 | ||||
rs17342717 | 6 | 25821542 | intron variant | C/T | snv | 6.1E-02 | 6 | ||||
rs3887266 | 0.925 | 0.120 | 6 | 25843518 | intron variant | C/T | snv | 8.9E-02 | 6 | ||
rs1150660 | 0.925 | 0.120 | 6 | 26101212 | upstream gene variant | A/C | snv | 0.73 | 5 |