Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs146486358
CUX1
0.882 0.080 7 102205168 missense variant C/T snv 8.6E-04 3.0E-04 3
rs3787283
SNAP25 ; SNAP25-AS1
0.882 0.040 20 10303770 intron variant A/G snv 0.34 3
rs3746544
SNAP25 ; SNAP25-AS1
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs11990063
MSRA
0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs1961982
C12orf42
0.925 0.040 12 103218955 intergenic variant G/A snv 0.27 2
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs10884216
LINC02627
0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 2
rs68081839
GRIA4
0.882 0.080 11 105762027 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT delins 3
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs35792458
XKR6
0.925 0.040 8 10964921 intron variant G/C snv 0.53 3
rs4839421
CYMP
0.925 0.040 1 110479338 intron variant C/A snv 0.40 3
rs17158930
DOCK4
0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs77826363 0.882 0.040 6 1128802 intergenic variant G/T snv 2.2E-02 3
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6276
DRD2
0.807 0.320 11 113410675 3 prime UTR variant C/T snv 0.54 8
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs10447760 0.851 0.040 7 114083210 upstream gene variant C/T snv 0.17 4
rs139459337
ZBTB20
0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs10809520 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 2
rs195478 0.925 0.040 6 115851928 intergenic variant C/A;G snv 2
rs7294919 0.851 0.080 12 116889787 regulatory region variant T/C snv 0.19 4
rs10233018 0.925 0.040 7 117883655 non coding transcript exon variant A/G snv 0.53 2