Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 2
rs771767 1.000 0.080 3 102029794 regulatory region variant A/G snv 0.70 2
rs9275292 1.000 0.120 6 32695512 intergenic variant C/A snv 0.53 2
rs10518765
UNC13C
1.000 0.040 15 54388434 intron variant A/C snv 0.16 1
rs11265260 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 1
rs1169286
HNF1A
1.000 0.080 12 120981253 intron variant T/C snv 0.39 1
rs12427353
HNF1A
1.000 0.080 12 120989098 intron variant G/A;C;T snv 1
rs12960928 1.000 0.080 18 60230570 intergenic variant T/C snv 0.21 1
rs1341665 1.000 0.080 1 159721769 intergenic variant G/A snv 0.32 1
rs3093068 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 1
rs876537
CRPP1
1.000 0.080 1 159705143 non coding transcript exon variant C/T snv 0.34 1
rs9268923
HLA-DRB9
1.000 0.040 6 32465058 intron variant C/T snv 0.29 1
rs12133641
IL6R
0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs1892534
LEPR
0.925 0.120 1 65640261 3 prime UTR variant C/T snv 0.44 3
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs13233571
BCL7B
0.925 0.120 7 73556901 intron variant C/T snv 9.2E-02 2
rs13244268
BAZ1B
0.925 0.120 7 73497513 intron variant T/C snv 9.2E-02 2
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 2
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 2
rs2524163
HLA-B
0.925 0.160 6 31291802 intron variant C/T snv 0.66 2
rs7305618
HNF1A-AS1
0.925 0.160 12 120965129 intron variant C/T snv 0.28 2
rs814295
GCKR
0.925 0.120 2 27520348 intron variant A/G snv 0.18 2
rs9378212 0.925 0.160 6 32477914 upstream gene variant C/G;T snv 2
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 1
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 1