Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
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
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 7
rs1329568 0.882 0.120 9 37037979 upstream gene variant T/A;G snv 6
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 6
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs17849502
NCF2 ; SMG7
0.827 0.240 1 183563445 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 3.4E-02 5
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs35677470
DNASE1L3
0.807 0.160 3 58197909 missense variant G/A;C snv 4.8E-02; 4.0E-06 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs74956615
FDX2 ; RAVER1
0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 5
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 4
rs4958880
TNIP1
0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs5754467
CCDC116 ; YDJC
0.851 0.160 22 21630805 upstream gene variant A/G;T snv 4