Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 5
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41 4
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 3
rs2900333
ATF7IP
0.882 0.200 12 14500933 3 prime UTR variant C/A;G;T snv 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs3744763
HNF1B
0.925 0.160 17 37730894 non coding transcript exon variant A/G snv 0.30 3
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 3
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50 2
rs1058205
KLK3
0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 2
rs17632542
KLK3
0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 2
rs266849
LOC105372441
0.925 0.080 19 50845834 intron variant G/A snv 0.82 2
rs266870
LOC105372441
1.000 0.080 19 50848678 intron variant T/C snv 0.43 2
rs16856139
SLC45A3
1.000 0.040 1 205669336 intron variant C/G;T snv 2
rs1991431
ZBTB38
3 141414608 intron variant G/A snv 0.50 2
rs10788160 10 121274035 intergenic variant G/A snv 0.19 1
rs11067228 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 1
rs1506684 19 50868163 intron variant A/G snv 0.53 1
rs10734875
ATF7IP
12 14389607 intron variant A/G;T snv 1
rs10772782
ATF7IP
12 14439909 intron variant A/G snv 0.29 1
rs11055956
ATF7IP
12 14381492 intron variant G/A;C snv 1
rs11055980
ATF7IP
1.000 0.040 12 14458588 intron variant C/T snv 0.40 1
rs2417349
ATF7IP
12 14428515 intron variant C/G;T snv 1
rs3213764
ATF7IP
0.925 0.080 12 14434367 missense variant A/G snv 0.47 0.42 1
rs4237951
ATF7IP
12 14471640 intron variant A/C snv 0.42 1