Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17228058
SMAD3
1.000 0.040 15 67157967 intron variant A/G snv 0.17 2
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 2
rs2169282 1.000 0.080 9 6350235 intergenic variant A/G snv 0.53 2
rs28393318
TLR10
1.000 0.080 4 38782646 intron variant A/G snv 0.29 2
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 2
rs34004019
HLA-DQB1-AS1
1.000 0.120 6 32658626 upstream gene variant A/G snv 0.29 2
rs367023
LINC00299
1.000 0.040 2 8309993 intron variant A/G snv 0.35 2
rs3787184
NFATC2
1.000 0.120 20 51541298 intron variant A/G snv 0.17 2
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38 2
rs61977073
TTC6
1.000 0.120 14 37682050 intron variant A/G snv 0.16 2
rs6738825
PLCL1
0.851 0.200 2 198032171 intron variant A/G snv 0.49 2
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 2
rs7705653 1.000 0.080 5 110807116 regulatory region variant A/G snv 0.29 2
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 2
rs10033073
STX18-AS1 ; LOC101928279
4 4773674 intron variant A/G snv 0.32 1
rs10486391
ITGB8
1.000 0.080 7 20336395 intron variant A/G snv 0.37 1
rs10957979 1.000 0.080 8 80377552 intron variant A/G snv 0.61 1
rs13395467
LINC00299
1.000 0.120 2 8311368 intron variant A/G snv 0.24 1
rs176095
PBX2 ; GPSM3
0.925 0.160 6 32190542 upstream gene variant A/G snv 0.22 1
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 1
rs2107357 16 27399508 upstream gene variant A/G snv 0.85 1
rs2589561 1.000 0.080 10 9004682 intergenic variant A/G snv 0.83 1
rs2910162
MIR3142HG
5 160482338 intron variant A/G snv 0.50 1
rs3806932
TSLP
0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51 1
rs4543123
TLR1
0.882 0.080 4 38790903 non coding transcript exon variant A/G snv 0.32 1