Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12497343 0.925 0.080 3 75330074 intron variant C/G;T snv 2
rs12527379 1.000 0.080 6 131958700 intron variant G/A snv 0.31 1
rs12591359 0.925 0.080 15 51247171 intron variant G/A snv 0.41 4
rs12733285 0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs12778366 0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs1287152741 0.925 0.080 5 80633984 missense variant C/T snv 8.0E-06 1.4E-05 2
rs1289280947 0.851 0.080 9 21974571 missense variant C/T snv 4.0E-06 5
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs12953717 0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs13254738 0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv 8
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs1342387 0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs1365611 0.925 0.080 4 174462542 intergenic variant C/T snv 0.28 2
rs1371367785 1.000 0.080 11 70206265 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1380087059
APC
0.882 0.160 5 112837749 missense variant G/C snv 4.0E-06 3
rs1383147053
DLD
0.882 0.120 7 107901762 missense variant G/A snv 4
rs1390282714 0.925 0.080 22 21769233 missense variant C/A;T snv 4.0E-06; 4.0E-06 2
rs14035
RAN
0.742 0.320 12 130876696 3 prime UTR variant C/T snv 0.33 15
rs1418586322 0.827 0.160 3 37050495 missense variant C/G snv 4.0E-06 6
rs1425164489 0.925 0.080 22 30617374 missense variant A/G;T snv 4.0E-06 2
rs1440032367 0.925 0.080 6 33189169 missense variant G/C snv 7.0E-06 3
rs1443465532 0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6