Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 1
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 1
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 3
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 3
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
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 4
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 3
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 2
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 1
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 10
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 6
rs11573156
PLA2G2A
0.882 0.240 1 19979653 5 prime UTR variant G/C snv 0.19 2