Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 1
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 1
rs11117432 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 1
rs11642873 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 1
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 1
rs3131917 0.882 0.080 5 173230018 upstream gene variant T/G snv 0.52 1
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 1
rs4342938 1.000 0.040 10 131557214 intergenic variant A/G snv 0.41 1
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 1
rs624988 0.925 0.120 1 116721168 regulatory region variant T/A;C snv 1
rs6832151 0.925 0.160 4 40301616 intergenic variant G/A;T snv 1
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 1
rs924080 0.882 0.240 1 67294457 intergenic variant T/C snv 0.45 1
rs1035798
AGER
1.000 0.040 6 32183445 splice region variant G/A snv 0.24 0.19 1
rs1535001
ANKS1A
0.925 0.080 6 34959503 intron variant A/G snv 0.47 1
rs3827644
ATG5
0.925 0.080 6 106237320 intron variant G/C snv 0.15 1
rs661968
AVEN ; CHRM5
1.000 0.040 15 33968868 5 prime UTR variant C/T snv 0.80 1
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs2409781
BLK
0.925 0.120 8 11502048 intron variant T/A;C snv 1
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs35677470
DNASE1L3
0.807 0.160 3 58197909 missense variant G/A;C snv 4.8E-02; 4.0E-06 1
rs11171747
ESYT1 ; ZC3H10
1.000 0.040 12 56124624 3 prime UTR variant T/A;G snv 1
rs4789182
GRB2
1.000 0.040 17 75378864 intron variant G/A snv 0.55 1
rs7763822
HLA-DPA2
1.000 0.040 6 33092651 intron variant C/T snv 5.4E-02 1
rs7764491
HLA-DPA2
1.000 0.040 6 33093063 non coding transcript exon variant C/G snv 5.4E-02 1