Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs994308 0.776 0.080 20 6622975 intergenic variant C/T snv 0.43 10
rs9939049
CDH1
0.790 0.080 16 68778398 intron variant A/T snv 0.29 9
rs9930005 0.776 0.080 16 80009361 intergenic variant C/A;T snv 10
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 9
rs9924886
CDH3
0.776 0.080 16 68710036 intron variant A/C snv 0.25 10
rs992157
TMBIM1 ; PNKD
0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 9
rs9901225
RETREG3
0.790 0.080 17 42603793 intron variant C/G;T snv 10
rs9834244 0.776 0.120 3 151704793 intergenic variant G/A snv 6.1E-02 10
rs983402 0.776 0.080 2 198916862 intron variant T/C snv 0.62 10
rs983318
LINC00511 ; LINC00673
0.776 0.080 17 72417112 intron variant G/A snv 0.18 10
rs9831861 0.790 0.080 3 53054269 intron variant T/G snv 0.53 9
rs9797885
TMEM91
0.790 0.080 19 41367096 intron variant A/G;T snv 9
rs9733843 0.790 0.080 10 8676041 intergenic variant A/G snv 0.24 9
rs964293 0.790 0.080 20 54200178 TF binding site variant C/A;T snv 9
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 9
rs9583269
MYO16
0.790 0.080 13 108630682 intron variant C/T snv 0.34 9
rs9537521
STARD13
0.790 0.080 13 33464043 intron variant G/A snv 0.20 9
rs9481067
SLC22A16
0.776 0.080 6 110429349 intron variant A/G snv 0.58 10
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
rs9409565
LOC107987100
0.790 0.080 9 94488752 intron variant C/G;T snv 9
rs9271770 0.776 0.120 6 32626471 upstream gene variant G/A snv 0.76 9
rs9271695 0.776 0.080 6 32625303 upstream gene variant A/G snv 0.76 10
rs899244 0.790 0.080 16 86666424 intron variant C/T snv 0.20 9
rs847208 0.790 0.080 16 86220445 downstream gene variant C/A snv 0.70 9
rs812481
LRIG1
0.790 0.080 3 66392011 intron variant C/G snv 0.66 9