Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs185819 0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 10
rs6457374 0.851 0.200 6 31304484 intron variant C/T snv 0.81 9
rs3823418 0.925 0.120 6 31133165 intron variant G/A snv 0.23 8
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 5
rs6457620 0.882 0.200 6 32696222 intergenic variant G/C snv 0.52 5
rs537160 0.882 0.240 6 31948623 intron variant A/G snv 0.73 4
rs2261033 0.925 0.160 6 31635814 non coding transcript exon variant A/G snv 0.42 3
rs2857693 1.000 0.120 6 31620607 upstream gene variant G/T snv 0.33 2
rs6930571 1.000 0.120 6 32415431 regulatory region variant G/T snv 0.13 2