Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11230815 11 61868654 downstream gene variant G/C;T snv 2
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 3
rs174449 11 61872907 downstream gene variant G/A snv 0.54 2
rs174626 11 61869585 downstream gene variant G/A snv 0.48 2
rs17764324 11 61867616 downstream gene variant G/A;T snv 2
rs17764935 11 61897285 downstream gene variant G/A snv 4.9E-02 3
rs17831757 11 61867728 downstream gene variant T/C snv 9.3E-02 2
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs422249 11 61872016 downstream gene variant T/C snv 0.67 2
rs4963452 11 62048331 downstream gene variant T/C snv 0.20 2
rs7104849 11 61870572 downstream gene variant G/A;T snv 2
rs7482316 11 61872726 downstream gene variant G/A;C snv 2
rs174468 11 61896219 upstream gene variant G/A snv 0.28 2
rs2521568 11 61933461 upstream gene variant G/C snv 9.5E-02 2
rs2727266 11 61936862 upstream gene variant A/G snv 9.8E-02 2
rs4246215 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs740006 11 61790396 3 prime UTR variant T/C snv 7.6E-02 2
rs174538 0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 21
rs174548 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs174550 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs412334 11 61792789 5 prime UTR variant C/T snv 0.10 2
rs7935946 11 61848070 5 prime UTR variant C/T snv 0.11 2
rs1109748 11 61955173 synonymous variant C/A snv 0.21 0.11 2
rs149803 11 61771548 synonymous variant C/G;T snv 0.18 2