Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 1
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 1
rs4888378
CFDP1
0.851 0.040 16 75298143 intron variant A/G snv 0.52 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 1
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 1
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 1
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 4
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 3
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 1