Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs2247056 0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6
rs2239804 0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs2395157 0.827 0.240 6 32380368 intron variant A/G snv 0.24 5
rs3817963 0.776 0.360 6 32400310 intron variant T/C snv 0.25 5
rs1480380 0.763 0.360 6 32945469 intron variant C/T snv 0.11 4
rs9257809 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 4
rs9268402 0.827 0.200 6 32373576 intron variant G/A snv 0.45 4
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs2239802 0.882 0.200 6 32444069 intron variant C/A;G;T snv 3
rs2239803 0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 3
rs3129888 0.882 0.240 6 32443949 intron variant G/A snv 0.82 0.80 3
rs3793126 0.882 0.240 6 32403842 intron variant A/G snv 0.24 3
rs6910071 0.790 0.320 6 32315077 intron variant A/G snv 0.14 3
rs9268403 0.807 0.240 6 32373696 intron variant T/C snv 0.24 3
rs1960278 0.925 0.160 6 31302097 intron variant C/G;T snv 2
rs2076522 0.925 0.160 6 32403402 intron variant G/C;T snv 2
rs2076524 0.925 0.160 6 32402907 intron variant A/G snv 0.26 0.24 2
rs2076525 0.925 0.160 6 32402839 intron variant T/C snv 0.24 2
rs2243868 0.925 0.160 6 31293499 intron variant A/G snv 0.66 2
rs2246954 0.925 0.160 6 31297485 intron variant A/G snv 0.60 2
rs2395153 0.925 0.160 6 32377818 intron variant C/G snv 0.34 2
rs2524052 0.925 0.160 6 31286219 intron variant A/G;T snv 2