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
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 4
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 3
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 3
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 2
rs1447352 11 92989595 downstream gene variant G/A snv 0.55 2
rs1495743 8 18415790 intergenic variant G/A;C snv 2
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 2
rs2216405 2 210752170 intergenic variant A/G snv 0.15 2
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 2
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 2
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 1
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs4329
ACE
17 63486097 intron variant A/C;G snv 2
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
rs13391552
ALMS1
2 73591809 intron variant G/A;C snv 2
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4