Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs145494032
CDKAL1
1.000 0.080 6 20665715 intron variant -/C delins 4.9E-05 1
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 3
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 3
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 3
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 3
rs12500426
PDLIM5
0.851 0.240 4 94593458 intron variant A/C snv 0.54 2
rs11873305 1.000 0.080 18 60381959 intron variant A/C snv 0.12 1
rs13083654
UBE2E2
1.000 0.080 3 23245193 intron variant A/C snv 0.11 1
rs1424642 1.000 0.080 2 57069423 intergenic variant A/C snv 0.78 1
rs16860234
IGF2BP2
0.925 0.080 3 185793096 intron variant A/C snv 0.33 1
rs2779772
CNTLN
1.000 0.080 9 17147193 intron variant A/C snv 0.21 1
rs2943640 1.000 0.080 2 226228869 intergenic variant A/C snv 0.75 1
rs4710940
CDKAL1
1.000 0.080 6 20657781 intron variant A/C snv 0.46 1
rs6593976
SLC26A9-AS1 ; SLC26A9
1.000 0.080 1 205940157 intron variant A/C snv 0.56 1
rs77464186
ARAP1
1.000 0.080 11 72749353 intron variant A/C snv 0.12 1
rs9358358
CDKAL1
1.000 0.080 6 20719162 intron variant A/C snv 0.19 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs7107217 0.882 0.160 11 129603795 intron variant A/C;G snv 2
rs6767484
IGF2BP2
1.000 0.080 3 185802790 intron variant A/C;G snv 1
rs7100710
CDC123
1.000 0.080 10 12208862 intron variant A/C;G snv 1
rs7628372
UBE2E2
1.000 0.080 3 23424764 intron variant A/C;G snv 1
rs9368216
CDKAL1
1.000 0.080 6 20654879 intron variant A/C;G snv 1
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 1