Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 27 | ||
rs1018381 | 0.882 | 0.040 | 6 | 15656839 | intron variant | G/A | snv | 0.16 | 6 | ||
rs1039049 | 1.000 | 0.040 | 4 | 80416472 | intron variant | G/A | snv | 0.98 | 1 | ||
rs1041536 | 1.000 | 0.040 | 20 | 9907627 | intergenic variant | T/C | snv | 0.46 | 1 | ||
rs10447760 | 0.851 | 0.040 | 7 | 114083210 | upstream gene variant | C/T | snv | 0.17 | 4 | ||
rs104886033 | 0.827 | 0.160 | 11 | 71444952 | start lost | T/C | snv | 1.2E-05; 4.0E-06 | 3.5E-05 | 10 | |
rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
rs104893878 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 21 | |||
rs1049564 | 0.882 | 0.160 | 14 | 20472447 | missense variant | G/A | snv | 0.19 | 0.21 | 6 | |
rs1051266 | 0.627 | 0.640 | 21 | 45537880 | missense variant | T/C;G | snv | 0.55; 4.4E-06 | 41 | ||
rs10521467 | 0.925 | 0.080 | 9 | 76036575 | intron variant | A/G | snv | 0.12 | 2 | ||
rs10524523 | 0.807 | 0.200 | 19 | 44899792 | intron variant | TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT | delins | 7 | |||
rs1057518813 | 0.790 | 0.240 | 13 | 102873305 | frameshift variant | CT/- | delins | 8 | |||
rs1057518907 | 0.732 | 0.320 | 20 | 58891811 | stop gained | C/G;T | snv | 16 | |||
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 72 | |
rs10748842 | 0.807 | 0.120 | 10 | 81889983 | intron variant | T/C | snv | 0.13 | 8 | ||
rs11030108 | 1.000 | 0.040 | 11 | 27673917 | intron variant | A/G | snv | 0.72 | 3 | ||
rs1108580 | 0.790 | 0.240 | 9 | 133639992 | splice region variant | A/G | snv | 0.45 | 0.54 | 9 | |
rs111231532 | 1.000 | 0.040 | 3 | 39135911 | intron variant | C/T | snv | 5.0E-02 | 1 | ||
rs11136000 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 19 | ||
rs111600634 | 1.000 | 0.040 | 9 | 117856347 | intron variant | T/G | snv | 1.5E-02 | 1 | ||
rs112422930 | 0.882 | 0.160 | 1 | 45332409 | missense variant | A/C | snv | 7.0E-06 | 4 | ||
rs1126680 | 0.851 | 0.160 | 3 | 165837337 | synonymous variant | C/T | snv | 5.6E-02 | 5.6E-02 | 5 | |
rs112961612 | 1.000 | 0.040 | 20 | 41872026 | intergenic variant | T/A | snv | 8.2E-02 | 1 | ||
rs113793030 | 1.000 | 0.040 | 10 | 70287104 | upstream gene variant | T/C | snv | 1.7E-02 | 1 |