Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs211718
SLC44A5
1 75640990 downstream gene variant T/C snv 0.75 3
rs2216405 2 210752170 intergenic variant A/G snv 0.15 2
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 4
rs2518049
AKR1C3
10 5095844 intron variant A/G;T snv 2
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
rs2624265
LINC02694
15 38856448 intron variant T/C snv 0.28 2
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs2652822
LACTB ; RPS27L
15 63130573 3 prime UTR variant T/C snv 0.41 2
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5
rs272889
SLC22A4 ; MIR3936HG
5 132329685 intron variant A/G snv 0.64 2
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 1
rs4149081
SLCO1B1
1.000 0.040 12 21225087 intron variant G/A snv 0.18 4
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 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
rs4481233
SLC2A9
0.925 0.120 4 9954455 intron variant C/T snv 0.16 5
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 2
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 2
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs503279
FUT2 ; LOC105447645
19 48705753 3 prime UTR variant T/C snv 0.48 2
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7