Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;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
rs13391552
ALMS1
2 73591809 intron variant G/A;C snv 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
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs2518049
AKR1C3
10 5095844 intron variant A/G;T snv 2
rs4329
ACE
17 63486097 intron variant A/C;G snv 2
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 2
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 3
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs2023634
DGCR9 ; DGCR5
22 18984937 intron variant A/G snv 7.9E-02 2
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 2
rs7094971
SLC16A9
0.925 0.120 10 59689806 intron variant A/G snv 0.13 4
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14 2
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 2