Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs1718119 0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306