Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3736228 0.752 0.400 11 68433827 missense variant C/T snv 0.13 0.11 13
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs2241767 0.763 0.440 3 186853407 intron variant A/G snv 0.10 10
rs290487 0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs316019 0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs2059806 0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 7