Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs132390
LOC105372985 ; EMID1
0.925 0.080 22 29225488 intron variant C/T snv 0.96 1
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 1
rs6556756
LOC105377703 ; LINC02143
0.882 0.160 5 164462274 intron variant G/T snv 0.89 2
rs1952246
RAD51B ; LOC105370546
1.000 0.080 14 68165095 intron variant G/A snv 0.89 1
rs1958115
RAD51B
1.000 0.080 14 68170948 intron variant C/A snv 0.89 1
rs2588814
RAD51B
1.000 0.080 14 68177081 intron variant G/A snv 0.87 1
rs2038979
RAD51B
1.000 0.080 14 68183059 intron variant G/A snv 0.87 1
rs2588819
LOC105370546 ; RAD51B
1.000 0.080 14 68161963 intron variant T/C snv 0.87 1
rs6472903
CASC9
0.925 0.080 8 75318066 intron variant G/T snv 0.86 1
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 1
rs2588808
RAD51B
1.000 0.080 14 68193464 intron variant A/G snv 0.84 1
rs2243905
LOC105370546 ; RAD51B
1.000 0.080 14 68166696 intron variant G/A snv 0.83 1
rs1550623 0.925 0.080 2 173348166 intron variant G/A snv 0.80 1
rs2588809
RAD51B
0.807 0.160 14 68193711 intron variant T/C snv 0.80 2
rs11075995
FTO
0.882 0.080 16 53821379 intron variant A/T snv 0.77 1
rs2180341
RNF146
0.882 0.160 6 127279485 intron variant G/A snv 0.73 2
rs7504990
DCC
0.851 0.120 18 52991406 intron variant T/C snv 0.73 1
rs4078288
DCC
0.882 0.120 18 53020881 intron variant G/A snv 0.73 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
rs704010
ZMIZ1
0.851 0.080 10 79081391 intron variant T/C snv 0.71 1
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 1
rs34330
CDKN1B ; GPR19
0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 1
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 1