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
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 13
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
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
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 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
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 6
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T 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
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 5
rs5743293
NOD2
0.807 0.200 16 50729868 frameshift variant C/-;CC delins 5
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs4077515
CARD9
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 4
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 4
rs7282490
GATD3A
0.882 0.080 21 44195858 intron variant G/A;T snv 4