Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1572072 1.000 0.120 13 23553071 intergenic variant G/T snv 0.36 1
rs1610588 1.000 0.120 6 29708939 upstream gene variant C/T snv 0.19 1
rs1610742 1.000 0.120 6 29710175 upstream gene variant T/C snv 0.19 1
rs28421666 1.000 0.120 6 32624960 upstream gene variant A/G snv 6.9E-02 1
rs29218 1.000 0.120 6 29639652 upstream gene variant A/G snv 0.17 1
rs3095267 1.000 0.120 6 29639269 upstream gene variant G/C;T snv 1
rs3095341 1.000 0.120 6 30758971 intron variant T/C snv 0.69 1
rs3129055 1.000 0.120 6 29702484 regulatory region variant A/G snv 0.24 1
rs3131866 1.000 0.120 6 29703963 downstream gene variant G/A snv 0.24 1
rs533550179 1.000 0.120 6 29714462 intergenic variant C/T snv 1
rs577078190 1.000 0.120 6 29716031 intergenic variant G/A snv 1
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 1
rs3757318
CCDC170
0.882 0.160 6 151592978 intron variant G/A snv 6.1E-02 1
rs3126085
FLG-AS1
0.851 0.280 1 152328341 intron variant G/A snv 0.29 1
rs29230
GABBR1
0.807 0.440 6 29608616 missense variant A/C;G snv 4.1E-06; 0.18 1
rs2517713
HLA-A
1.000 0.120 6 29950322 downstream gene variant G/A;T snv 1
rs2860580
HLA-A
1.000 0.120 6 29938914 upstream gene variant A/C;G;T snv 1
rs2975042
HLA-A
1.000 0.120 6 29952759 upstream gene variant G/A;T snv 1
rs3869062
HLA-A
1.000 0.120 6 29967114 downstream gene variant A/G snv 5.5E-02 1
rs5009448
HLA-A
1.000 0.120 6 29972711 upstream gene variant T/C snv 0.74 1
rs9260484
HLA-A
1.000 0.120 6 29952476 upstream gene variant A/C snv 0.62 1
rs9260734
HLA-A
1.000 0.120 6 29964889 intergenic variant G/A snv 0.22 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs169111
ITGA9
1.000 0.120 3 37474042 intron variant C/T snv 0.84 1
rs169188
ITGA9
1.000 0.120 3 37465958 intron variant G/A snv 7.6E-02 1