Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1789924 0.925 0.160 4 99353129 upstream gene variant C/G;T snv 4
rs1612735 1.000 0.080 4 99336850 intron variant T/C snv 0.31 3
rs1614972 0.925 0.160 4 99336998 intron variant C/T snv 0.38 3
rs12639833 1.000 0.080 4 99346215 intron variant C/T snv 0.31 3
rs2241894 1.000 0.080 4 99344976 synonymous variant T/A;C snv 4.0E-06; 0.30 3