Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 7
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 3
rs6934903 0.925 0.080 6 135130426 intergenic variant T/A snv 0.14 2
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 2
rs7606173
BCL11A
1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 2
rs11968814 1.000 0.080 6 71067268 intergenic variant G/A snv 4.4E-02 1
rs3864785 1.000 0.080 9 7603506 intergenic variant G/C snv 0.89 1
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 1
rs10172646
BCL11A
1.000 0.080 2 60493622 intron variant G/A snv 0.64 1
rs10195871
BCL11A
1.000 0.080 2 60493454 intron variant A/G;T snv 1
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 1
rs1427407
BCL11A
0.827 0.120 2 60490908 intron variant T/C;G snv 1
rs1896294
BCL11A
1.000 0.080 2 60491939 intron variant C/G;T snv 1
rs1896295
BCL11A
1.000 0.080 2 60496951 intron variant T/C snv 0.81 1
rs1896296
BCL11A
1.000 0.080 2 60496952 intron variant G/T snv 0.80 1
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 1
rs6545816
BCL11A
1.000 0.080 2 60487726 intron variant A/C;G snv 0.50 1
rs6545817
BCL11A
1.000 0.080 2 60488044 intron variant C/T snv 0.49 1