Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11230563 0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 8
rs17824933
CD6
1.000 0.080 11 60993140 intron variant C/A;G snv 1
rs112852289 1.000 0.080 11 61008833 frameshift variant -/T ins 5.1E-06; 5.1E-06 1
rs2074225 1.000 0.080 11 61008834 missense variant C/T snv 0.53 0.58 1
rs386754116 1.000 0.080 11 61008834 missense variant CG/TC mnv 1