Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 2
rs12988520
UGT1A6 ; UGT1A9 ; UGT1A8 ; UGT1A10 ; UGT1A7
1.000 0.040 2 233698748 intron variant A/C snv 0.51 2
rs8179252
GCKR
0.882 0.120 2 27523965 downstream gene variant A/C snv 0.37 2
rs295
LPL
1.000 0.040 8 19958727 intron variant A/C snv 0.28 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs1441756 1.000 0.040 8 20010875 intergenic variant A/C;G;T snv 1
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 1
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 1
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs486394
LINC02702
1.000 0.040 11 116655605 intron variant A/C;T snv 3
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 1
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 6
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 5
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 5
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 4
rs6494005
ALDH1A2 ; LIPC
1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38 4