Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2301249 | 15 | 74800043 | intron variant | T/C | snv | 0.66 | 3 | ||||
rs2306363 | 11 | 65638129 | 5 prime UTR variant | G/T | snv | 0.15 | 7 | ||||
rs2484294 | 10 | 114032303 | intergenic variant | G/A | snv | 0.70 | 4 | ||||
rs2521501 | 0.925 | 0.080 | 15 | 90894158 | intron variant | A/C;T | snv | 10 | |||
rs2681485 | 12 | 89631845 | intron variant | G/A;T | snv | 3 | |||||
rs2681492 | 0.925 | 0.040 | 12 | 89619312 | intron variant | T/C;G | snv | 10 | |||
rs35441 | 12 | 115115310 | intergenic variant | C/T | snv | 0.40 | 5 | ||||
rs3753584 | 0.827 | 0.080 | 1 | 11804529 | 5 prime UTR variant | T/C | snv | 0.14 | 10 | ||
rs381815 | 1.000 | 0.040 | 11 | 16880721 | intron variant | C/A;T | snv | 0.24 | 6 | ||
rs419076 | 3 | 169383098 | intron variant | T/A;C | snv | 6 | |||||
rs438885 | 2 | 164195781 | intron variant | A/T | snv | 0.56 | 5 | ||||
rs448378 | 1.000 | 0.040 | 3 | 169383111 | intron variant | G/A;C | snv | 5 | |||
rs4590817 | 10 | 61707795 | intron variant | G/C | snv | 0.15 | 5 | ||||
rs4759319 | 12 | 54030947 | intron variant | G/C;T | snv | 4 | |||||
rs5883070 | 7 | 27240226 | intron variant | -/AAAACA;AACA | delins | 0.91 | 5 | ||||
rs6015450 | 20 | 59176062 | intron variant | A/G | snv | 0.14 | 7 | ||||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 10 | |||
rs656319 | 8 | 9956901 | intergenic variant | A/G | snv | 0.49 | 3 | ||||
rs7310615 | 0.882 | 12 | 111427245 | intron variant | C/G | snv | 0.67 | 12 | |||
rs7577262 | 2 | 233910224 | intergenic variant | G/A;T | snv | 4 | |||||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 13 |