Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs543874 | 1.000 | 0.080 | 1 | 177920345 | upstream gene variant | A/G | snv | 0.21 | 2 | ||
rs591120 | 1 | 177933618 | missense variant | G/A;C | snv | 4.0E-06; 0.42 | 2 | ||||
rs10913469 | 1.000 | 0.080 | 1 | 177944384 | intron variant | T/C | snv | 0.22 | 5 | ||
rs1516725 | 0.925 | 0.120 | 3 | 186106215 | intron variant | T/C | snv | 0.86 | 3 | ||
rs7647305 | 1.000 | 0.080 | 3 | 186116501 | intron variant | T/C | snv | 0.74 | 3 | ||
rs9816226 | 1.000 | 0.080 | 3 | 186116710 | intron variant | A/T | snv | 0.82 | 3 | ||
rs13034723 | 2 | 190120954 | intron variant | G/A | snv | 0.37 | 2 | ||||
rs12444979 | 1.000 | 0.080 | 16 | 19922278 | intergenic variant | C/T | snv | 0.11 | 2 | ||
rs4633 | 0.695 | 0.400 | 22 | 19962712 | synonymous variant | C/T | snv | 0.46 | 0.45 | 2 | |
rs12597579 | 16 | 20246545 | intergenic variant | C/A;T | snv | 2 | |||||
rs9368219 | 1.000 | 0.080 | 6 | 20674460 | intron variant | C/T | snv | 0.19 | 3 | ||
rs9356744 | 0.882 | 0.120 | 6 | 20685255 | intron variant | T/C | snv | 0.42 | 3 | ||
rs7766070 | 1.000 | 0.080 | 6 | 20686342 | intron variant | C/A | snv | 0.25 | 3 | ||
rs9368222 | 1.000 | 0.080 | 6 | 20686765 | intron variant | C/A;T | snv | 5 | |||
rs2206734 | 0.882 | 0.160 | 6 | 20694653 | intron variant | C/T | snv | 0.20 | 3 | ||
rs7800783 | 7 | 21731847 | intron variant | G/A | snv | 5.9E-02 | 2 | ||||
rs2943634 | 0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv | 4 | |||
rs7374732 | 1.000 | 0.080 | 3 | 23161963 | regulatory region variant | C/T | snv | 0.73 | 1 | ||
rs7586879 | 2 | 24894108 | intron variant | C/T | snv | 0.47 | 2 | ||||
rs6545814 | 2 | 24908447 | intron variant | A/G | snv | 0.53 | 2 | ||||
rs11676272 | 1.000 | 0.040 | 2 | 24918669 | missense variant | A/G | snv | 0.47 | 0.57 | 2 | |
rs713586 | 0.925 | 0.160 | 2 | 24935139 | intergenic variant | T/C | snv | 0.58 | 2 | ||
rs1561288 | 2 | 25146133 | 3 prime UTR variant | C/T | snv | 0.29 | 2 | ||||
rs12999687 | 2 | 25289569 | intron variant | T/G | snv | 0.48 | 2 | ||||
rs10261878 | 7 | 25910925 | intergenic variant | A/C | snv | 0.80 | 2 |