Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs2721800
MPP6
0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs2391769
LOC105378866
0.925 0.040 1 96513405 regulatory region variant A/G;T snv 3
rs10492664 0.925 0.040 13 108163877 intergenic variant C/A;T snv 2
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 2
rs145108385
LOC648987
0.925 0.040 5 43054645 intron variant A/G snv 2
rs1476535
FOXP2
0.925 0.040 7 114430980 intron variant C/G;T snv 2
rs227283
MANBA
0.925 0.120 4 102686096 intron variant C/G;T snv 2
rs4259397 0.925 0.040 8 92354062 upstream gene variant G/A;T snv 2
rs4916723
LINC00461
0.925 0.040 5 88558577 intron variant A/C;G;T snv 2
rs56037433
SLC4A10
0.925 0.040 2 161719475 intron variant G/A;T snv 2
rs58502974
ADCY2
0.925 0.040 5 7755787 intron variant T/A;G snv 2
rs7094182 0.925 0.120 10 8484656 intergenic variant G/A;C snv 2
rs10514604
ATP2C2
1.000 0.040 16 84412778 intron variant C/A;G snv 1
rs11074889
EMP2
1.000 0.040 16 10539308 intron variant A/G;T snv 1
rs11317767
LOC105371529
1.000 0.040 17 8770824 intergenic variant TTT/-;TT;TTTT delins 1
rs114181198 1.000 0.040 2 183618431 intergenic variant C/A snv 1
rs11591402
SORCS3
1.000 0.040 10 104987596 intron variant T/A;G snv 1
rs12036759 1.000 0.040 1 232789695 regulatory region variant A/G;T snv 1
rs12042052 1.000 0.040 1 232799973 upstream gene variant A/C;G;T snv 1
rs12671878
LOC107986722 ; DPP6
1.000 0.040 7 153861864 intergenic variant C/A;T snv 1
rs1329650
HECTD2-AS1
0.882 0.080 10 91588363 regulatory region variant G/A;T snv 1