Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 6
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 2
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs10923931
NOTCH2
0.925 0.120 1 119975336 intron variant G/T snv 0.17 2
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs1800574
HNF1A ; HNF1A-AS1
0.882 0.080 12 120979061 missense variant C/T snv 2.9E-02 2.2E-02 1
rs2464196
HNF1A
0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 2
rs12779790 0.882 0.120 10 12286011 intergenic variant A/G snv 0.17 2
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 2
rs10229583 1.000 0.080 7 127606849 downstream gene variant G/A snv 0.23 1
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 2
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 3
rs9348440
CDKAL1
1.000 0.080 6 20641105 intron variant C/T snv 0.13 2
rs6456368
CDKAL1
1.000 0.080 6 20659575 intron variant T/C snv 0.40 2