Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs793607
DUBR
1.000 0.080 3 107340876 intron variant G/A;C snv 2
rs7705653 1.000 0.080 5 110807116 regulatory region variant A/G snv 0.29 2
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 3
rs1814576 5 110824180 intergenic variant T/C snv 7.0E-02 1
rs6869502 5 110830384 intergenic variant A/T snv 0.28 1
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 2
rs3806932
TSLP
0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51 1
rs3806933
TSLP
0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40 1
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 2
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 4
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs12935657
CLEC16A
0.925 0.080 16 11125184 intron variant G/A snv 0.18 2
rs11645657
LOC105371081 ; CLEC16A
1.000 0.080 16 11129597 intron variant C/A;G snv 0.48 2
rs36045143
LOC105371081 ; CLEC16A
1.000 0.080 16 11131109 intron variant A/G snv 0.18 3
rs7203459
LOC105371081 ; CLEC16A
1.000 0.080 16 11136846 intron variant T/C snv 0.23 2
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs13403656
SOCAR ; MIR4435-2HG
2 111511550 intron variant A/T snv 0.84 1
rs659529 1.000 0.080 11 111566171 downstream gene variant T/A;C snv 2
rs7130753 11 111599843 upstream gene variant C/T snv 0.37 1
rs4848612
ANAPC1
2 111630961 non coding transcript exon variant G/A snv 0.74 1
rs11644510
CLEC16A
1.000 0.120 16 11183501 downstream gene variant C/T snv 0.39 2
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 1
rs12596613
LOC400499
16 11397150 intron variant C/G snv 0.29 1