Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 10
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 9
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 7
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 6
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 6
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5