Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs17102823 0.776 0.080 14 34894698 intergenic variant A/C;G snv 10
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 6
rs11574938
ITGAL
0.827 0.120 16 30474072 missense variant G/A;C snv 0.62 6
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs1267499
LOC101928354
0.807 0.160 6 14715651 intron variant T/A;C snv 6
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 6
rs2227551
PLAU
0.827 0.120 10 73909432 intron variant G/C;T snv 6
rs2497318 0.827 0.120 10 92672243 upstream gene variant C/A;T snv 6
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 6
rs4921482
LOC285626
0.807 0.120 5 159337470 intron variant T/C;G snv 6
rs4946717
PRDM1
0.827 0.120 6 106026874 intron variant C/A;G;T snv 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 6
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv 6
rs71559680 0.827 0.120 6 21430497 intergenic variant TAG/CAT mnv 6
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 6