Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1586840 1.000 0.080 12 19909563 intron variant G/A snv 0.96 1
rs132390
LOC105372985 ; EMID1
0.925 0.080 22 29225488 intron variant C/T snv 0.96 2
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 2
rs6556756
LOC105377703 ; LINC02143
0.882 0.160 5 164462274 intron variant G/T snv 0.89 3
rs6472903
CASC9
0.925 0.080 8 75318066 intron variant G/T snv 0.86 2
rs1550623 0.925 0.080 2 173348166 intron variant G/A snv 0.80 2
rs2588809
RAD51B
0.807 0.160 14 68193711 intron variant T/C snv 0.80 2
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs2435357
RET
0.790 0.240 10 43086608 intron variant T/C snv 0.79 3
rs11075995
FTO
0.882 0.080 16 53821379 intron variant A/T snv 0.77 2
rs7166081 0.925 0.080 15 67199963 downstream gene variant G/A snv 0.76 4
rs3116494
CD28
0.882 0.120 2 203727298 intron variant G/A snv 0.76 2
rs421379 0.925 0.080 5 91979496 intergenic variant T/C snv 0.75 1
rs2180341
RNF146
0.882 0.160 6 127279485 intron variant G/A snv 0.73 3
rs7504990
DCC
0.851 0.120 18 52991406 intron variant T/C snv 0.73 2
rs4078288
DCC
0.882 0.120 18 53020881 intron variant G/A snv 0.73 1
rs9306160
RRP1B
0.925 0.080 21 43687681 missense variant T/C snv 0.69 0.73 2
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 1
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 2
rs5743810
TLR6 ; TLR1
0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs704010
ZMIZ1
0.851 0.080 10 79081391 intron variant T/C snv 0.71 2
rs1477196
FTO
0.851 0.200 16 53774346 intron variant A/G snv 0.71 2
rs527616
AQP4-AS1
0.851 0.080 18 26757460 intron variant C/G snv 0.71 2
rs34330
CDKN1B ; GPR19
0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 1