Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs994856
DGKH
0.925 0.040 13 42134315 intron variant A/G snv 0.37 2
rs993137
CADM2
1.000 0.040 3 85449885 intron variant C/G;T snv 1
rs993136
CADM2
1.000 0.040 3 85450183 intron variant T/C snv 0.52 1
rs9882911
TRANK1
1.000 0.040 3 36843901 intron variant T/C snv 0.36 1
rs9882879 1.000 0.040 3 36802580 intergenic variant C/T snv 0.31 1
rs9876421 1.000 0.040 3 36806825 intergenic variant C/T snv 0.31 1
rs9875793 0.925 0.080 3 170968784 intron variant A/G snv 0.14 3
rs9862857
LOC101927995 ; LOC105377013
0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs9829032
CADM2
0.925 0.080 3 85634450 intron variant A/G snv 0.41 2
rs9821223
TRANK1
1.000 0.040 3 36841878 intron variant T/C snv 0.36 1
rs9811916
TRANK1
1.000 0.040 3 36836595 intron variant A/G snv 0.38 1
rs9804190
ANK3
0.882 0.040 10 60080073 intron variant C/T snv 0.30 5
rs976498 1.000 0.040 16 64687040 intergenic variant C/G;T snv 1
rs968847 0.925 0.040 10 114998320 downstream gene variant G/T snv 0.20 2
rs967771
GABRB2
0.925 0.080 5 161335167 intron variant C/T snv 0.16 2
rs9662615
CSMD2
1.000 0.040 1 34138966 intron variant C/T snv 0.41 1
rs9633553
LOC107984292 ; ANK3
1.000 0.040 10 60514979 intron variant T/G snv 8.3E-02 1
rs9608816
ASCC2
0.925 0.040 22 29820911 intron variant C/A snv 0.49 2
rs9577511
GRTP1
0.882 0.040 13 113337508 intron variant A/G snv 0.15 4
rs9567552
BRCA2
0.925 0.040 13 32316090 5 prime UTR variant G/A;T snv 2
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs9558571
DAOA-AS1 ; DAOA
0.882 0.040 13 105486017 intron variant C/T snv 0.28 3
rs954129
TENM4
1.000 0.040 11 79349751 intron variant T/A snv 0.18 1