Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9271597 0.925 0.080 6 32623514 upstream gene variant T/A snv 0.39 1
rs9295822 1.000 0.040 6 29861103 intron variant C/T snv 0.12 1
rs9295871 1.000 0.040 6 30443312 intergenic variant T/C snv 0.17 1
rs9295873 1.000 0.040 6 30446458 upstream gene variant A/G snv 0.17 1
rs9295886 1.000 0.040 6 30453620 intron variant C/T snv 0.17 1
rs9461612 1.000 0.040 6 30470779 downstream gene variant G/A snv 0.16 1
rs9501336 1.000 0.040 6 30459733 downstream gene variant G/A snv 0.17 1
rs9501447 1.000 0.040 6 30430063 intergenic variant A/G snv 0.17 1
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 1
rs17195551
ATAT1
1.000 0.040 6 30633618 intron variant C/T snv 3.2E-02 1
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 1
rs3814231
CASP7
1.000 0.040 10 113721259 intron variant C/T snv 0.23 1
rs3130455
CCHCR1 ; TCF19
1.000 0.040 6 31158201 5 prime UTR variant A/C;T snv 1
rs291700
CDK5RAP1
0.925 0.040 20 33394043 synonymous variant T/C snv 0.64 0.62 1
rs16872571
CLNK
0.925 0.080 4 10725229 intergenic variant C/T snv 0.33 1
rs7746003
DDR1-DT
1.000 0.040 6 30875117 non coding transcript exon variant T/A snv 3.1E-02 1
rs2523505
DDX39B ; ATP6V1G2-DDX39B ; DDX39B-AS1 ; SNORD84
1.000 0.040 6 31542225 5 prime UTR variant C/G snv 7.6E-02 1
rs3130347
EGFL8 ; PPT2-EGFL8 ; PPT2
1.000 0.040 6 32166879 intron variant T/C snv 0.15 0.18 1
rs9926296
FANCA
1.000 0.040 16 89751681 intron variant A/G snv 0.54 1
rs6902119
FGFR1OP
0.882 0.160 6 167092303 intron variant T/C;G snv 1
rs17008723
FOXP1
0.925 0.040 3 71523984 intron variant T/G snv 0.15 1
rs17190134
HCG22
1.000 0.040 6 31054083 non coding transcript exon variant C/A;G snv 1
rs3823355
HCG9 ; HLA-A
1.000 0.040 6 29974306 upstream gene variant C/A;T snv 1
rs12206499
HLA-A
1.000 0.040 6 29969350 downstream gene variant A/G snv 0.27 1
rs9468925
HLA-B
0.851 0.040 6 31291060 intron variant G/A snv 0.44 1