Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs2285809
HECTD4
1.000 0.120 12 112270622 intron variant T/C snv 0.16 1
rs10774654 1.000 0.120 12 112525756 intergenic variant A/G snv 0.20 1
rs10850053 1.000 0.120 12 112539973 regulatory region variant T/C snv 0.19 1
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs12566340
AP4B1-AS1 ; BCL2L15
0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 1
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 2
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 2
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs12679857
COLEC10
1.000 0.120 8 118965098 intergenic variant A/G snv 0.36 1
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs4505848
KIAA1109
0.776 0.400 4 122211337 intron variant A/G snv 0.29 2
rs17388568
ADAD1
0.827 0.280 4 122408207 intron variant G/A snv 0.20 3
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs9388489
CENPW
0.925 0.160 6 126377573 intron variant A/G;T snv 2
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8