Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5
rs4149081
SLCO1B1
1.000 0.040 12 21225087 intron variant G/A snv 0.18 4
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 4
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs10885409
TCF7L2
1.000 0.080 10 113048313 intron variant T/C snv 0.54 1
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 1
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 1
rs9358356
CDKAL1
1.000 0.080 6 20667151 intron variant T/C snv 0.39 1
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs4481233
SLC2A9
0.925 0.120 4 9954455 intron variant C/T snv 0.16 5
rs7094971
SLC16A9
0.925 0.120 10 59689806 intron variant A/G snv 0.13 4
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 3
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 2
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 2
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 4
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 3
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 2
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6