Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 14
rs1359880314
SLC19A1
0.763 0.320 21 45534541 synonymous variant C/T snv 1.6E-05 2.8E-05 12
rs79204362
CYP1B1
0.763 0.120 2 38071251 missense variant C/T snv 5.8E-03 1.7E-03 10
rs7650466
EPHA3
0.851 0.200 3 89481208 3 prime UTR variant C/T snv 0.23 7
rs57865060
CYP1B1-AS1 ; CYP1B1
0.827 0.160 2 38074704 missense variant C/T snv 1.1E-02 5.7E-03 6
rs104894381
TBX5
0.925 0.120 12 114401830 missense variant C/T snv 5
rs527236031
PIGT ; MIR6812
0.882 0.080 20 45424323 missense variant C/T snv 1.6E-05 4.2E-05 5
rs1052108705
TCF19 ; POU5F1
6 31165217 missense variant C/T snv 4.1E-06 2.1E-05 3
rs768746587
TCF19 ; POU5F1
6 31165136 missense variant C/T snv 8.4E-06 3
rs756434709
NOTCH1
9 136514670 missense variant C/T snv 2.0E-05 7.0E-06 2
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs368087026
SLC19A1
0.637 0.520 21 45530890 missense variant G/A snv 33
rs1057519320
FBN1
0.807 0.160 15 48444574 missense variant G/A snv 7
rs587777570
KIF5C
1.000 2 148947018 missense variant G/A snv 4
rs1057517786
PDCD10
0.925 0.400 3 167704889 stop gained G/A snv 3
rs121918214
FTO
1.000 0.200 16 53873837 missense variant G/A snv 4.0E-06 7.0E-06 3
rs201968272
DDX11
0.925 0.160 12 31089147 missense variant G/A snv 3
rs745616565
FTO
1.000 0.200 16 53873855 missense variant G/A snv 1.6E-05 2.1E-05 3
rs774753616
PIGT ; LOC107985405
1.000 20 45419351 missense variant G/A snv 1.2E-05 1.4E-05 3
rs1387329667
NOTCH1
9 136500595 missense variant G/A snv 2
rs764120087
EP300
22 41117439 missense variant G/A snv 8.0E-06 2
rs1801198
TCN2
0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs201405525
DECR1
0.925 0.240 8 90044993 missense variant G/A;C snv 4.5E-04; 4.0E-06 3