Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 64 | ||
rs4588 | 0.597 | 0.720 | 4 | 71752606 | missense variant | G/A;T | snv | 1.6E-05; 0.25 | 53 | ||
rs2282679 | 0.645 | 0.480 | 4 | 71742666 | intron variant | T/G | snv | 0.21 | 38 | ||
rs10741657 | 0.637 | 0.520 | 11 | 14893332 | upstream gene variant | A/G | snv | 0.65 | 34 | ||
rs12785878 | 0.677 | 0.520 | 11 | 71456403 | intron variant | G/A;T | snv | 25 | |||
rs2060793 | 0.776 | 0.240 | 11 | 14893764 | upstream gene variant | A/G | snv | 0.63 | 11 | ||
rs1993116 | 0.827 | 0.200 | 11 | 14888688 | intron variant | A/G | snv | 0.65 | 8 | ||
rs3829251 | 0.851 | 0.120 | 11 | 71483513 | intron variant | G/A | snv | 0.21 | 8 | ||
rs17216707 | 20 | 54115823 | intergenic variant | T/C | snv | 0.17 | 6 | ||||
rs3755967 | 0.925 | 0.080 | 4 | 71743681 | intron variant | C/A;T | snv | 6 | |||
rs6127099 | 20 | 54114863 | intergenic variant | A/T | snv | 0.28 | 5 | ||||
rs11234027 | 0.882 | 0.080 | 11 | 71523061 | intron variant | G/A | snv | 0.24 | 5 | ||
rs12800438 | 1.000 | 0.080 | 11 | 71459957 | non coding transcript exon variant | G/A;T | snv | 5 | |||
rs17467825 | 0.925 | 0.080 | 4 | 71739800 | downstream gene variant | A/G | snv | 0.22 | 4 | ||
rs1155563 | 0.925 | 0.080 | 4 | 71777771 | intron variant | T/A;C | snv | 4 | |||
rs78862524 | 4 | 72305473 | intron variant | C/A | snv | 3.9E-02 | 3 | ||||
rs10485165 | 6 | 88403098 | intron variant | C/G;T | snv | 3 | |||||
rs2302190 | 17 | 58507147 | missense variant | T/A;C | snv | 0.24 | 3 | ||||
rs11586313 | 1 | 152917994 | TF binding site variant | G/A;C | snv | 0.51 | 2 | ||||
rs117300835 | 11 | 15097429 | intergenic variant | G/A | snv | 7.6E-03 | 2 | ||||
rs12287212 | 11 | 14428315 | intergenic variant | C/A | snv | 0.31 | 2 | ||||
rs12868495 | 13 | 34067425 | intergenic variant | G/A | snv | 2.3E-02 | 2 | ||||
rs138485827 | 4 | 72166226 | intergenic variant | C/T | snv | 5.0E-02 | 2 | ||||
rs1410656 | 13 | 46968386 | intergenic variant | T/C | snv | 0.97 | 2 | ||||
rs148189294 | 4 | 71575200 | downstream gene variant | G/A | snv | 2.6E-02 | 2 |