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
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs10518693
IVD
15 40407823 intron variant C/T snv 0.37 2
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2
rs10885409
TCF7L2
1.000 0.080 10 113048313 intron variant T/C snv 0.54 1
rs11185790
PANK1
10 89612776 intron variant G/A snv 0.15 2
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs12670403
LOC101927609 ; AHR
7 17269655 intron variant C/A snv 0.46 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 2
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs13391552
ALMS1
2 73591809 intron variant G/A;C snv 2
rs1447352 11 92989595 downstream gene variant G/A snv 0.55 2
rs1495743 8 18415790 intergenic variant G/A;C snv 2
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 1
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 3
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 2
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs2023634
DGCR9 ; DGCR5
22 18984937 intron variant A/G snv 7.9E-02 2
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv 3
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4
rs2087160
ENPEP
4 110413574 intron variant G/T snv 0.68 2