Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs11230815 11 61868654 downstream gene variant G/C;T snv 2
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 2
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 2
rs17831757 11 61867728 downstream gene variant T/C snv 9.3E-02 2
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
rs10220265 13 103397233 downstream gene variant G/A snv 0.28 1
rs12526913 6 11082691 downstream gene variant A/G;T snv 1
rs12665478 6 11080592 downstream gene variant G/A snv 0.41 1
rs16832011
LCT
2 135787729 downstream gene variant A/G snv 5.1E-02 1
rs1692120 11 61650000 downstream gene variant G/A snv 0.43 1
rs174627 11 61869994 downstream gene variant G/A snv 0.10 1
rs2945816 11 56094615 downstream gene variant T/C snv 1
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
rs3758977 11 61969772 upstream gene variant T/A;G snv 1
rs8012543 14 28618344 upstream gene variant G/A snv 0.50 1