Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 6
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 4
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 2
rs3135002 1.000 0.120 6 32700662 TF binding site variant A/C snv 0.80 2
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs229533
C1QTNF6
1.000 0.120 22 37191071 intron variant A/C snv 0.50 1
rs3095340 1.000 0.120 6 30759162 intron variant A/C snv 0.16 1
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 1
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 1
rs4948088 0.925 0.160 7 50959497 intron variant A/C snv 0.96 1
rs917911
CD69
1.000 0.120 12 9753255 3 prime UTR variant A/C snv 0.29 1
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs3957148 0.925 0.160 6 32714360 upstream gene variant A/C;G snv 0.10 3
rs7679475
LOC107986309
0.925 0.120 4 121392885 intergenic variant A/C;G snv 2
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs539514
LMO7
1.000 0.120 13 75752146 intron variant A/C;T snv 1
rs6476839
GLIS3
0.925 0.120 9 4290823 intron variant A/C;T snv 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15