Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2293581
GREM1 ; LOC100131315
0.776 0.080 15 32718535 5 prime UTR variant G/A;C snv 0.27 10
rs34405347 0.776 0.080 9 98917470 regulatory region variant T/C;G snv 10
rs45597035
KLF5
0.776 0.080 13 73075014 intron variant A/G;T snv 10
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 10
rs4968127
NXN
0.776 0.080 17 906403 intron variant G/A;T snv 10
rs6066825
PREX1
0.776 0.080 20 48723580 intron variant A/G;T snv 10
rs61389091
CHRDL2
0.776 0.080 11 74716876 intron variant C/G;T snv 10
rs6678517
LAMC1
0.776 0.080 1 183033504 intron variant A/G;T snv 10
rs7121958
POLD3
0.776 0.080 11 74568967 intron variant T/A;G snv 10
rs7708610 0.776 0.080 5 40102341 intergenic variant G/A;C snv 10
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 10
rs9901225
RETREG3
0.790 0.080 17 42603793 intron variant C/G;T snv 10
rs9930005 0.776 0.080 16 80009361 intergenic variant C/A;T snv 10
rs10152518 0.790 0.080 15 67884824 intergenic variant G/A;T snv 9
rs10951878 0.790 0.080 7 46887097 downstream gene variant C/A;T snv 9
rs12255141
VTI1A
0.790 0.080 10 112535133 intron variant A/G;T snv 9
rs12412391
LINC01475
0.790 0.080 10 99529178 intron variant A/G;T snv 9
rs12682374
POU5F1B ; PCAT1 ; CCAT2 ; CASC8
0.790 0.080 8 127398703 intron variant C/A;G;T snv 9
rs1330889
LINC00446 ; OBI1-AS1
0.790 0.080 13 78035480 intron variant T/A;C snv 9
rs1445011 0.790 0.080 5 40280100 intergenic variant T/C;G snv 9
rs16959063
FMN1 ; LOC107984089
0.790 0.080 15 32813529 intron variant G/A;C snv 9
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv 9
rs2070699
EDN1
0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 9
rs254563
C5orf66
0.790 0.080 5 135104736 intron variant G/A;C snv 9
rs2696839 0.790 0.080 16 86306842 intergenic variant G/A;C snv 9