Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801280 0.716 0.440 8 18400344 missense variant T/C snv 0.38 0.39 14
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs861530 0.732 0.320 14 103707786 3 prime UTR variant T/C snv 0.65 13
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6869366 0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18