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
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
rs4495487 0.925 0.080 9 5072798 intron variant T/C snv 0.23 3
rs10815148 0.882 0.080 9 5057284 intron variant T/A snv 0.33 3
rs12339666 0.925 0.080 9 5063296 intron variant G/T snv 0.34 2
rs3808850 0.925 0.080 9 4983311 upstream gene variant T/A;C snv 2
rs121912473 0.925 0.080 9 5070026 missense variant AA/TT mnv 2
rs7046736 0.925 0.080 9 5015732 intron variant C/A snv 0.39 2