Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 6
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 6
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 6
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 4
rs2523578 1.000 6 31360765 upstream gene variant G/A snv 0.79 4
rs6457620 0.882 0.200 6 32696222 intergenic variant G/C snv 0.52 4
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv 4
rs1865760
SLC17A2
0.925 0.120 6 25916751 synonymous variant C/T snv 0.42 0.34 4
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 3
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 3
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3