Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs10821936 0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs7089424 0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs1057519753 0.763 0.120 1 64846664 missense variant C/A snv 9