Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 181
rs10974944 0.882 0.160 9 5070831 intron variant C/G snv 0.25 4
rs12342421 0.851 0.080 9 5065750 intron variant G/C snv 0.23 4
rs10974947 0.882 0.080 9 5072846 intron variant G/A snv 0.23 3
rs10815148 0.882 0.080 9 5057284 intron variant T/A snv 0.33 3