Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 1
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 1
rs12731740
MIR29B2CHG
1 207851475 intron variant C/T snv 9.1E-02 1
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 1
rs2235529
WNT4
1.000 0.040 1 22123994 intron variant C/T snv 0.13 1
rs2820464
LYPLAL1-AS1
1 219519878 intergenic variant G/A;C snv 1
rs4846567 1 219577375 regulatory region variant G/T snv 0.23 1
rs505102
CFH
1 196650372 upstream gene variant T/C snv 0.40 1
rs6701231
TBX15
1 118953038 intron variant C/A;G snv 1
rs984222
TBX15
1 118961220 intron variant C/A;G snv 1
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 3
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs1020731
RBMS1
1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 1
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 1
rs9750952 1.000 0.080 2 238827723 intergenic variant C/T snv 0.19 1
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 3
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 3
rs4686340
SRGAP3
3 9303534 intron variant A/C snv 0.80 1
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1
rs6784615
NISCH
1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 1