Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs6499165
SLC7A6OS ; SLC7A6
16 68292297 non coding transcript exon variant A/C snv 0.80 2
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 1
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv 3
rs4329
ACE
17 63486097 intron variant A/C;G snv 2
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
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
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5
rs7094971
SLC16A9
0.925 0.120 10 59689806 intron variant A/G snv 0.13 4
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 4
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2
rs2023634
DGCR9 ; DGCR5
22 18984937 intron variant A/G snv 7.9E-02 2
rs2216405 2 210752170 intergenic variant A/G snv 0.15 2
rs272889
SLC22A4 ; MIR3936HG
5 132329685 intron variant A/G snv 0.64 2
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 2
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 2
rs2518049
AKR1C3
10 5095844 intron variant A/G;T snv 2
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
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 4
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 3