Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2106261 0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs16899974 0.827 0.120 5 34998772 missense variant C/A snv 0.24 0.19 5
rs1273246817 0.882 0.080 1 237784169 missense variant A/C snv 3