Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1001007
CCR5AS
0.827 0.120 3 46387167 intron variant A/G;T snv 5
rs1004234
LINC02863 ; IRF1-AS1
0.827 0.120 5 132421409 intron variant A/G;T snv 5
rs10889676
IL23R
0.827 0.120 1 67256884 intron variant C/A;T snv 5
rs11098964
ANTXR2
0.827 0.120 4 79966815 intron variant A/G;T snv 5
rs11306716 0.827 0.120 2 203843041 intergenic variant T/-;TT delins 5
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 5
rs11750385
LINC02213
0.827 0.120 5 10521556 intron variant G/A;T snv 5
rs1333062
ITLN1
0.807 0.200 1 160876494 downstream gene variant T/C;G snv 5
rs141992399
CARD9 ; DNLZ
0.827 0.120 9 136365140 splice donor variant C/G;T snv 3.3E-03; 4.0E-06 5
rs196941
ERN1
0.827 0.120 17 64069832 non coding transcript exon variant G/C;T snv 5
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 5
rs28550029
SKAP2
0.827 0.120 7 26832962 intron variant C/A;T snv 5
rs34670647 0.827 0.120 16 30159695 regulatory region variant T/- delins 5