Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs6457374 0.851 0.200 6 31304484 intron variant C/T snv 0.81 9
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 8
rs13101828 0.851 0.160 4 971932 intron variant A/G snv 0.43 6