Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10788038 10 120117008 intergenic variant T/C snv 0.61 1
rs12340987 9 85156012 upstream gene variant A/G snv 0.19 1
rs13271368 8 125493898 intron variant C/T snv 0.18 1
rs17064002 13 42996665 upstream gene variant C/T snv 1.8E-02 1
rs17138114 6 4379277 intron variant A/G snv 0.10 1
rs2960051 18 30276169 intergenic variant C/T snv 0.84 1
rs4432842 1.000 0.080 5 57876251 intergenic variant T/C snv 0.45 1
rs4564656 18 30301067 intron variant G/A snv 0.76 1
rs6508654 18 30302598 intron variant T/C snv 0.81 1
rs7742369 6 34197944 TF binding site variant A/G snv 0.30 1
rs7968682 12 65978100 intergenic variant G/T snv 0.56 1
rs930811 9 2696555 intergenic variant G/A snv 0.47 1
rs9883204
ADCY5
3 123377973 intron variant T/A;C snv 1
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 1
rs798489
GNA12 ; AMZ1
7 2762169 splice donor variant C/T snv 0.20 1
rs7780752
GNGT1
7 93612328 intron variant T/C snv 0.27 1
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv 1
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 1
rs2928148
INO80
15 41109352 intron variant G/A snv 0.44 1
rs11867479
KCNJ16
17 70094066 intron variant C/A;T snv 1
rs1415701
L3MBTL3
6 130024690 intron variant G/A snv 0.31 1
rs925098
LCORL
4 17918188 intron variant G/A snv 0.70 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs3107997
LOC105372047 ; LOC105372046
18 30340278 intron variant C/T snv 0.21 1
rs809871
LOC105374986
6 26256298 downstream gene variant C/G;T snv 1