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
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 10
rs863750 12 124020897 intron variant C/T snv 0.53 7
rs55747707 7 73623036 intron variant G/A snv 0.16 5
rs72959041 6 127133748 intron variant G/A snv 3.2E-02 5
rs10049088 3 157079859 upstream gene variant C/T snv 0.35 3
rs11216183 11 116910829 intron variant C/A snv 0.10 3
rs12437696 15 40586276 upstream gene variant A/G snv 0.51 3
rs2306589 17 36493030 non coding transcript exon variant T/C snv 0.49 3