Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 1
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 1
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 1
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 1
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 1
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 1
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 1
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 1
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
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
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
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 1
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 1
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 1
rs6666258
KCNN3
0.882 0.080 1 154841792 intron variant G/C snv 0.30 1
rs11781551
LOC105375733
1.000 0.040 8 122395852 intergenic variant G/A snv 0.40 1
rs17045031
LOC105377142
1.000 0.040 3 66717940 intergenic variant G/A snv 0.10 1
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 1
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 1
rs4380028
MORF4L1
0.807 0.120 15 78818751 intron variant C/T snv 0.34 1