Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs2070699
EDN1
0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 14
rs7025417
LOC107987046 ; IL33
0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50 9
rs1989839
ZMYND10 ; RASSF1
0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20 8
rs1872328
ACYP2
0.827 0.120 2 54168122 intron variant G/A snv 7.3E-02 6
rs1005464
BMP2
0.882 0.040 20 6775501 intron variant G/A snv 0.19 5
rs4150441
ERCC3
0.882 0.040 2 127283339 intron variant T/C snv 0.37 5
rs6973569
NPSR1-AS1
0.851 0.080 7 34583412 intron variant G/A snv 4.7E-02 5
rs8103851
PRKCG
0.851 0.040 19 53894400 intron variant C/G snv 0.44 5
rs12602273
TP53
0.851 0.080 17 7679695 intron variant C/G snv 0.15 4
rs16948627
ITGA3
0.882 0.040 17 50063432 intron variant C/A;T snv 4
rs1906953
GRM4
0.882 0.040 6 34068669 intron variant C/T snv 0.25 4
rs4150506
ERCC3
0.851 0.120 2 127262970 intron variant G/A snv 0.18 4
rs4789223
SMIM6 ; RECQL5
0.851 0.120 17 75645819 intron variant G/A snv 0.46 4
rs7034162
NFIB
0.882 0.040 9 14190288 intron variant A/T snv 0.81 4
rs7646409
PIK3CA
0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs1295925
VMP1
0.882 0.040 17 59832902 intron variant T/C snv 0.60 3
rs2075559
COL1A1
0.882 0.040 17 50189930 intron variant G/A;C;T snv 0.52; 4.0E-06 3