Source: CURATED ×
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
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
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 5
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
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
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
rs954129
TENM4
1.000 0.040 11 79349751 intron variant T/A snv 0.18 1
rs951266
CHRNA5
0.882 0.080 15 78586199 intron variant G/A snv 0.26 4
rs9401634 1.000 0.040 6 98130635 intron variant T/C snv 0.41 1
rs9396756 1.000 0.040 6 17160887 intergenic variant G/A;C;T snv 1
rs9393813
ZNF204P
1.000 0.040 6 27363817 upstream gene variant C/A;T snv 1
rs9388171 1.000 0.040 6 98127850 intron variant C/G snv 0.44 1
rs9385269 1.000 0.040 6 98100103 intron variant C/T snv 0.44 1
rs9378249 0.925 0.160 6 31359924 upstream gene variant T/A;G snv 3