Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs2479409
PCSK9
1.000 0.040 1 55038977 upstream gene variant G/A snv 0.66 3
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs3019885
SLC30A8
0.925 0.120 8 117013406 intron variant T/A;G snv 2
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 1
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 1
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 1
rs7025486
DAB2IP
0.851 0.040 9 121660124 intron variant G/A snv 0.28 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs1466535
LRP1
0.790 0.160 12 57140687 intron variant G/A;C snv 1
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 1