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 | ||
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 | ||
rs1993116 | 0.827 | 0.200 | 11 | 14888688 | intron variant | A/G | snv | 0.65 | 8 | ||
rs17467825 | 0.925 | 0.080 | 4 | 71739800 | downstream gene variant | A/G | snv | 0.22 | 4 | ||
rs1007392 | 11 | 14753045 | intron variant | A/G | snv | 0.35 | 2 | ||||
rs117865811 | 11 | 14180763 | intron variant | A/G | snv | 6.3E-03 | 2 | ||||
rs1526692 | 4 | 71713007 | intergenic variant | A/G | snv | 0.41 | 2 | ||||
rs185378533 | 11 | 71422087 | intron variant | A/G | snv | 0.68 | 2 | ||||
rs2277458 | 14 | 39114277 | 5 prime UTR variant | A/G | snv | 0.80 | 0.83 | 2 | |||
rs6127099 | 20 | 54114863 | intergenic variant | A/T | snv | 0.28 | 5 | ||||
rs78862524 | 4 | 72305473 | intron variant | C/A | snv | 3.9E-02 | 3 | ||||
rs12287212 | 11 | 14428315 | intergenic variant | C/A | snv | 0.31 | 2 | ||||
rs3755967 | 0.925 | 0.080 | 4 | 71743681 | intron variant | C/A;T | snv | 6 | |||
rs843005 | 4 | 71750610 | intron variant | C/A;T | snv | 2 | |||||
rs10485165 | 6 | 88403098 | intron variant | C/G;T | snv | 3 | |||||
rs55665837 | 11 | 14473503 | intron variant | C/G;T | snv | 2 | |||||
rs10745742 | 12 | 95964751 | intron variant | C/T | snv | 0.48 | 2 | ||||
rs138485827 | 4 | 72166226 | intergenic variant | C/T | snv | 5.0E-02 | 2 | ||||
rs3819817 | 12 | 95984993 | intron variant | C/T | snv | 0.50 | 2 | ||||
rs4423214 | 11 | 71462208 | intron variant | C/T | snv | 0.58 | 2 | ||||
rs79666294 | 5 | 155047146 | regulatory region variant | C/T | snv | 2.2E-02 | 2 | ||||
rs3829251 | 0.851 | 0.120 | 11 | 71483513 | intron variant | G/A | snv | 0.21 | 8 | ||
rs11234027 | 0.882 | 0.080 | 11 | 71523061 | intron variant | G/A | snv | 0.24 | 5 | ||
rs116970203 | 11 | 14855172 | intron variant | G/A | snv | 2.2E-02 | 2 |