Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3736228
LRP5
0.752 0.400 11 68433827 missense variant C/T snv 0.13 0.11 13
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 9
rs9533156
TNFSF11
0.807 0.280 13 42573535 intron variant T/C snv 0.47 8
rs1864325
MAPT
0.882 0.160 17 45900461 intron variant C/T snv 0.14 6
rs4355801 0.882 0.120 8 118911634 regulatory region variant A/G;T snv 5
rs7524102 0.882 0.160 1 22371954 intergenic variant A/G snv 0.21 5
rs9921222
AXIN1
0.925 0.120 16 325782 intron variant C/T snv 0.51 5
rs6959212 7 38088724 intergenic variant T/C;G snv 4
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 4
rs3755955
IDUA
0.925 0.080 4 1000626 missense variant G/A;C snv 0.16; 8.0E-06 4
rs7521902
LOC105376850
1.000 0.040 1 22164231 intergenic variant C/A snv 0.22 4
rs4985155
PDXDC1
16 15035602 intron variant A/G snv 0.40 0.37 4
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 4
rs2908004
WNT16
1.000 0.040 7 121329715 missense variant G/A;T snv 0.44; 4.0E-06 4
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 3
rs1564981 16 50952397 intergenic variant G/A snv 0.60 3
rs6426749 1.000 0.080 1 22384980 intergenic variant G/C snv 0.19 3
rs6532023 1.000 0.080 4 87852697 regulatory region variant T/G snv 0.66 3
rs9525638 13 42554441 regulatory region variant T/C snv 0.37 3
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32 3
rs917727
FAM3C
7 121378525 intron variant C/A;T snv 0.33 3
rs1054627
IBSP
1.000 0.080 4 87811540 missense variant G/A snv 0.30 0.24 3
rs2273061
JAG1
1.000 0.080 20 10658895 intron variant G/A snv 0.46 3
rs9533090
LINC02341
13 42377313 intron variant C/T snv 0.39 3
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57 3