Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 3
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 2
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 16
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 3
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 2
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 2
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 2
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 2
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs2411884
KCNQ1
11 2714304 intron variant C/A;G snv 2
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16