Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 13
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 6
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 3
rs8087799 0.882 0.080 18 22605468 regulatory region variant G/A snv 0.43 3
rs919433
ANKRD44 ; ANKRD44-IT1
0.882 0.080 2 197301841 intron variant G/A snv 0.38 3
rs7866503
CDKN2B-AS1
0.882 0.080 9 22091925 intron variant G/T snv 0.50 3
rs595244
FBN1
0.882 0.080 15 48548638 intron variant C/T snv 7.7E-02 3
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 3
rs12133641
IL6R
0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 2
rs2479409
PCSK9
1.000 0.040 1 55038977 upstream gene variant G/A snv 0.66 2
rs1795061 1.000 0.040 1 214235937 intergenic variant T/C;G snv 1
rs9316871 1.000 0.040 13 22287782 intergenic variant A/G snv 0.22 1
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 1