Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs117865811 | 11 | 14180763 | intron variant | A/G | snv | 6.3E-03 | 2 | ||||
rs182244780 | 11 | 14363985 | intron variant | G/A | snv | 6.0E-03 | 2 | ||||
rs12287212 | 11 | 14428315 | intergenic variant | C/A | snv | 0.31 | 2 | ||||
rs55665837 | 11 | 14473503 | intron variant | C/G;T | snv | 2 | |||||
rs1007392 | 11 | 14753045 | intron variant | A/G | snv | 0.35 | 2 | ||||
rs11023332 | 11 | 14762564 | intron variant | G/C | snv | 0.35 | 2 | ||||
rs116970203 | 11 | 14855172 | intron variant | G/A | snv | 2.2E-02 | 2 | ||||
rs117913124 | 11 | 14879385 | synonymous variant | G/A | snv | 1.7E-02 | 1.6E-02 | 2 | |||
rs1993116 | 0.827 | 0.200 | 11 | 14888688 | intron variant | A/G | snv | 0.65 | 8 | ||
rs10741657 | 0.637 | 0.520 | 11 | 14893332 | upstream gene variant | A/G | snv | 0.65 | 34 | ||
rs2060793 | 0.776 | 0.240 | 11 | 14893764 | upstream gene variant | A/G | snv | 0.63 | 11 | ||
rs117300835 | 11 | 15097429 | intergenic variant | G/A | snv | 7.6E-03 | 2 | ||||
rs11586313 | 1 | 152917994 | TF binding site variant | G/A;C | snv | 0.51 | 2 | ||||
rs79666294 | 5 | 155047146 | regulatory region variant | C/T | snv | 2.2E-02 | 2 | ||||
rs6730714 | 2 | 222184302 | intergenic variant | G/A;T | snv | 2 | |||||
rs2207173 | 20 | 22824423 | intergenic variant | G/A | snv | 0.72 | 2 | ||||
rs156299 | 7 | 24185113 | intergenic variant | T/G | snv | 0.53 | 2 | ||||
rs12868495 | 13 | 34067425 | intergenic variant | G/A | snv | 2.3E-02 | 2 | ||||
rs8018720 | 14 | 39086981 | missense variant | G/C;T | snv | 0.80; 1.1E-04 | 2 | ||||
rs2277458 | 14 | 39114277 | 5 prime UTR variant | A/G | snv | 0.80 | 0.83 | 2 | |||
rs719700 | 12 | 45635426 | intergenic variant | T/C | snv | 1.8E-02 | 2 | ||||
rs1410656 | 13 | 46968386 | intergenic variant | T/C | snv | 0.97 | 2 | ||||
rs6127099 | 20 | 54114863 | intergenic variant | A/T | snv | 0.28 | 5 | ||||
rs17216707 | 20 | 54115823 | intergenic variant | T/C | snv | 0.17 | 6 | ||||
rs2302190 | 17 | 58507147 | missense variant | T/A;C | snv | 0.24 | 3 |