Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs11172113 0.882 0.080 12 57133500 intron variant T/C snv 0.42 10
rs344781 0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 7
rs1835740 0.882 0.040 8 97154685 intergenic variant T/C snv 0.75 5
rs2651899 0.882 0.040 1 3167148 intron variant T/A;C snv 5
rs12134493 0.925 0.040 1 115135325 TF binding site variant C/A snv 9.2E-02 4