Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 2
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs9885413 0.925 0.040 5 110840429 intergenic variant G/T snv 0.19 1
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs737337
DOCK6
0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 3
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 2
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 16
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs189919070
MIR4788
1.000 0.040 3 134436825 upstream gene variant C/A;T snv 3
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs4528684 1.000 0.040 19 14240762 intergenic variant C/T snv 0.12 1
rs139130723 1.000 0.040 6 14411553 intergenic variant A/G snv 4.4E-03 3
rs142803096 1.000 0.040 6 14420151 intergenic variant G/C snv 4.4E-03 3
rs149447933
LOC101928331 ; LOC105374942
1.000 0.040 6 14453908 intron variant C/G snv 4.4E-03 3
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 2