Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1000005 | 21 | 33060745 | intron variant | G/C | snv | 0.51 | 1 | ||||
rs10000770 | 1.000 | 0.040 | 4 | 142693109 | intron variant | C/T | snv | 0.11 | 1 | ||
rs1000096 | 4 | 38691214 | intron variant | C/T | snv | 0.39 | 1 | ||||
rs1000113 | 0.925 | 0.040 | 5 | 150860514 | intron variant | C/T | snv | 0.13 | 1 | ||
rs10001414 | 1.000 | 0.040 | 4 | 168569930 | intron variant | A/G | snv | 1.7E-02 | 1 | ||
rs10001545 | 4 | 87254878 | intergenic variant | C/A;T | snv | 3 | |||||
rs10002082 | 4 | 164159753 | intron variant | A/G | snv | 0.20 | 1 | ||||
rs10002111 | 4 | 66949786 | regulatory region variant | A/G | snv | 0.82 | 1 | ||||
rs10002854 | 1.000 | 0.040 | 4 | 7519419 | intron variant | C/T | snv | 8.8E-02 | 1 | ||
rs10004892 | 1.000 | 0.040 | 4 | 188951696 | intergenic variant | T/C | snv | 0.21 | 1 | ||
rs10005067 | 4 | 87931491 | intergenic variant | T/A;C | snv | 1 | |||||
rs10005233 | 1.000 | 0.040 | 4 | 89822180 | 3 prime UTR variant | C/T | snv | 0.58 | 0.59 | 1 | |
rs10005540 | 4 | 173660916 | downstream gene variant | C/G;T | snv | 1 | |||||
rs1000579 | 1.000 | 0.080 | 4 | 4717767 | intron variant | A/G | snv | 0.44 | 3 | ||
rs1000597 | 0.925 | 0.120 | 7 | 30897563 | intron variant | T/A;C | snv | 2 | |||
rs10006108 | 1.000 | 0.040 | 4 | 97002862 | intergenic variant | C/T | snv | 0.48 | 1 | ||
rs10006235 | 1.000 | 0.040 | 4 | 129748953 | non coding transcript exon variant | T/C | snv | 0.73 | 2 | ||
rs10006237 | 4 | 136606920 | intergenic variant | C/T | snv | 0.50 | 1 | ||||
rs10006327 | 1.000 | 0.080 | 4 | 102969823 | intron variant | T/A;C | snv | 1 | |||
rs10006418 | 1.000 | 0.040 | 4 | 142691588 | intron variant | A/T | snv | 0.11 | 1 | ||
rs10007052 | 1.000 | 0.040 | 4 | 141084419 | intron variant | C/A | snv | 0.31 | 1 | ||
rs1000708 | 1.000 | 0.160 | 12 | 59689707 | intron variant | C/T | snv | 0.58 | 1 | ||
rs10007186 | 4 | 78667891 | intron variant | C/T | snv | 0.65 | 1 | ||||
rs1000791 | 17 | 79269796 | intron variant | T/A | snv | 8.2E-02 | 1 | ||||
rs10007975 | 4 | 99527667 | intron variant | C/T | snv | 0.27 | 1 |