Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1532624 0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs11643718 0.807 0.240 16 56899607 missense variant G/A snv 0.11 8.4E-02 10
rs7679 0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 9
rs4783961 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 7