Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs61750420 0.689 0.480 7 92501562 missense variant C/T snv 3.2E-04 3.5E-04 52
rs28934906 0.716 0.320 X 154031355 missense variant G/A snv 46
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 37
rs180177035 0.752 0.280 7 140801502 missense variant T/C snv 35
rs28934908 0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 23
rs113994097 0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs3740066 0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs387906799 0.742 0.200 2 240788118 missense variant G/A snv 19
rs398123009 0.790 0.200 11 66211206 missense variant C/T snv 7.0E-06 19
rs267607165 0.708 0.520 16 89935679 missense variant G/A;C snv 18
rs267607048 0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 16
rs587777308 0.763 0.040 5 161873196 missense variant G/A snv 14
rs387907281 0.752 0.280 19 41970284 missense variant C/T snv 13
rs536289169 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs1554032789 0.925 0.160 5 37048547 missense variant T/A snv 13
rs80338758 0.790 0.400 X 71127367 missense variant C/A;T snv 12
rs2273697 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 11
rs4846049 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs796052676 0.807 0.200 8 132180246 missense variant G/A snv 10