Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7726159 | 0.790 | 0.160 | 5 | 1282204 | intron variant | C/A | snv | 0.29 | 10 | ||
rs13428812 | 0.827 | 0.120 | 2 | 25269598 | intron variant | A/G | snv | 0.31 | 9 | ||
rs246079 | 0.790 | 0.120 | 12 | 109109255 | intron variant | A/G;T | snv | 9 | |||
rs1989969 | 0.827 | 0.120 | 12 | 47884227 | intron variant | A/C;G;T | snv | 0.60 | 8 | ||
rs2303426 | 0.790 | 0.080 | 2 | 47403411 | intron variant | C/A;G;T | snv | 1.9E-05; 0.47 | 8 | ||
rs3819102 | 0.827 | 0.120 | 18 | 675307 | intron variant | A/G | snv | 4.5E-02 | 3.6E-02 | 8 | |
rs41291957 | 0.882 | 0.200 | 5 | 149428827 | intron variant | G/A | snv | 0.12 | 7 | ||
rs6504950 | 0.807 | 0.120 | 17 | 54979110 | intron variant | G/A | snv | 0.29 | 7 | ||
rs7664413 | 0.851 | 0.160 | 4 | 176687553 | intron variant | C/T | snv | 0.24 | 0.25 | 7 | |
rs798766 | 0.851 | 0.120 | 4 | 1732512 | intron variant | T/C | snv | 0.76 | 6 | ||
rs9471643 | 0.882 | 0.080 | 6 | 41751177 | intron variant | G/C | snv | 0.19 | 6 | ||
rs4919743 | 0.925 | 0.080 | 12 | 52915800 | intron variant | G/A | snv | 0.13 | 5 | ||
rs12740674 | 0.882 | 0.080 | 1 | 68121775 | intron variant | C/T | snv | 0.34 | 4 | ||
rs13254990 | 0.882 | 0.120 | 8 | 128064205 | intron variant | C/T | snv | 0.24 | 4 | ||
rs6458238 | 0.882 | 0.080 | 6 | 41749967 | intron variant | G/A;C | snv | 4 | |||
rs2001389 | 0.925 | 0.120 | 10 | 102615501 | intron variant | G/A;C | snv | 3 | |||
rs2046463 | 1.000 | 0.080 | 4 | 176681548 | intron variant | G/A;C | snv | 3 | |||
rs4635002 | 0.925 | 0.080 | 10 | 127064415 | intron variant | A/C | snv | 0.92 | 3 | ||
rs5999749 | 0.925 | 0.080 | 22 | 21833371 | intron variant | A/C;T | snv | 3 | |||
rs7853122 | 0.925 | 0.080 | 9 | 131705224 | intron variant | C/T | snv | 0.87 | 3 | ||
rs11777210 | 1.000 | 0.080 | 8 | 1979843 | intron variant | C/G;T | snv | 2 | |||
rs1670661 | 1.000 | 0.040 | 11 | 21209124 | intron variant | C/G;T | snv | 2 | |||
rs11646171 | 16 | 61824185 | intron variant | G/A | snv | 0.13 | 1 | ||||
rs169724 | 9 | 90828217 | intron variant | T/C;G | snv | 1 | |||||
rs182361 | 9 | 90828077 | intron variant | C/A | snv | 0.11 | 1 |