Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1035142 | 0.807 | 0.200 | 2 | 201288355 | 3 prime UTR variant | T/C;G | snv | 0.54 | 7 | ||
rs1036199 | 0.925 | 0.160 | 5 | 157104725 | missense variant | C/A | snv | 0.87 | 0.83 | 3 | |
rs1041885 | 1.000 | 0.120 | 6 | 32445032 | 3 prime UTR variant | T/A | snv | 0.15 | 1 | ||
rs1042127 | 0.925 | 0.120 | 6 | 31116393 | missense variant | A/C | snv | 0.21 | 0.17 | 2 | |
rs1042337 | 1.000 | 0.120 | 6 | 32937204 | missense variant | G/A | snv | 0.78 | 0.80 | 1 | |
rs1042448 | 1.000 | 0.120 | 6 | 33086565 | 3 prime UTR variant | T/A;C | snv | 6.1E-03; 7.4E-06 | 1 | ||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs1042544 | 0.925 | 0.200 | 6 | 33086680 | 3 prime UTR variant | A/G | snv | 0.38 | 2 | ||
rs1042663 | 0.925 | 0.160 | 6 | 31937353 | synonymous variant | G/A | snv | 9.7E-02 | 0.12 | 3 | |
rs1043099 | 1.000 | 0.120 | 22 | 30285268 | 3 prime UTR variant | C/A;G;T | snv | 1 | |||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs1046080 | 1.000 | 0.120 | 6 | 31628105 | missense variant | C/A | snv | 0.79 | 0.74 | 2 | |
rs10461703 | 1.000 | 0.120 | 5 | 33596119 | intron variant | C/G;T | snv | 1 | |||
rs10468473 | 1.000 | 0.120 | 17 | 12224359 | intergenic variant | T/C | snv | 8.8E-02 | 1 | ||
rs10484544 | 1.000 | 0.120 | 6 | 29027942 | upstream gene variant | T/C | snv | 0.22 | 1 | ||
rs10484554 | 0.807 | 0.200 | 6 | 31306778 | intron variant | C/T | snv | 0.12 | 11 | ||
rs10484560 | 1.000 | 0.120 | 6 | 32330360 | intron variant | G/A | snv | 8.6E-02 | 1 | ||
rs10484565 | 0.925 | 0.200 | 6 | 32827255 | 3 prime UTR variant | G/A | snv | 6.1E-02 | 2 | ||
rs10484566 | 0.925 | 0.200 | 6 | 32867481 | regulatory region variant | T/G | snv | 6.8E-02 | 2 | ||
rs10488631 | 0.742 | 0.280 | 7 | 128954129 | upstream gene variant | T/C | snv | 9.0E-02 | 13 | ||
rs104895218 | 0.827 | 0.240 | 12 | 6334099 | missense variant | C/T | snv | 5 | |||
rs104895219 | 0.827 | 0.240 | 12 | 6333823 | missense variant | G/A;T | snv | 5 | |||
rs104895221 | 0.925 | 0.200 | 12 | 6333490 | missense variant | A/G | snv | 2 | |||
rs104895271 | 0.851 | 0.240 | 12 | 6334161 | missense variant | A/C;G | snv | 1.6E-04; 4.8E-05 | 6 | ||
rs10489629 | 0.827 | 0.240 | 1 | 67222666 | intron variant | T/C | snv | 0.48 | 5 |