Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 7
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 6
rs367569
LOC105371082 ; RMI2
0.807 0.120 16 11271643 intron variant C/T snv 0.32 6
rs28998802
NOS2
0.807 0.120 17 27797882 intron variant G/A snv 0.11 6
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36 6
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 5
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs9988642
IL23R
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 3
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 3
rs1250544
ZMIZ1
0.882 0.080 10 79273128 intron variant G/A snv 0.32 3
rs12884468 0.925 0.040 14 35383280 downstream gene variant T/C snv 0.47 2
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 2
rs4683946 0.925 0.080 3 101896982 intron variant G/T snv 0.19 2
rs2675662
CAMK2G
0.925 0.040 10 73839369 intron variant A/G snv 0.55 2
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv 2
rs3802826
ETS1
0.925 0.040 11 128536543 non coding transcript exon variant A/G;T snv 2
rs17716942
KCNH7
0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 2
rs62149416
LINC01185
0.925 0.040 2 60856371 intron variant T/C snv 0.26 2
rs7637230
LINC02085
0.925 0.040 3 101944711 intron variant A/G;T snv 2