Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs798489
GNA12 ; AMZ1
7 2762169 splice donor variant C/T snv 0.20 1
rs809871
LOC105374986
6 26256298 downstream gene variant C/G;T snv 1
rs925098
LCORL
4 17918188 intron variant G/A snv 0.70 1
rs930811 9 2696555 intergenic variant G/A snv 0.47 1
rs9883204
ADCY5
3 123377973 intron variant T/A;C snv 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 1
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 1
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs3740360
PLCE1
0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 1
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 2
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 1
rs9366778
LINC02571 ; LOC112267902 ; HLA-B
0.925 0.120 6 31301396 intron variant G/A snv 0.47 6
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 3
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27 3
rs2421016
PLEKHA1
0.925 0.120 10 122407996 intron variant C/T snv 0.46 2
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 2
rs2292626
PLEKHA1
0.925 0.120 10 122427198 intron variant C/T snv 0.46 1
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 3