Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 7
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 6
rs729761
LOC105375069 ; LOC107986598
0.925 0.120 6 43836834 intron variant T/A;G snv 6
rs149454410
SLC2A9
0.925 0.120 4 9942000 missense variant C/G;T snv 4.0E-05; 3.2E-04 5
rs186459505
SFMBT1
0.925 0.120 3 52907083 missense variant G/A;T snv 1.1E-04; 4.0E-06 5
rs7422339
CPS1
1.000 0.080 2 210675783 missense variant C/A snv 5
rs11554266
GNAS
1.000 0.040 20 58903791 splice region variant C/G;T snv 4.0E-06; 2.3E-03 4
rs141310123
NFATC1
0.925 0.120 18 79411390 missense variant C/A;T snv 2.1E-04; 4.8E-06 4
rs201874364
ETV5
1.000 0.040 3 186065822 missense variant C/A;T snv 4.0E-06; 7.2E-05 4
rs202007714
SLC25A26 ; LRIG1
1.000 0.040 3 66383098 missense variant G/A;C snv 1.4E-04; 4.0E-06 4
rs2279463
SLC22A2
1.000 0.080 6 160247357 intron variant A/G;T snv 4
rs2337106
SMAD7
18 48934533 intron variant C/A;G snv 4
rs2467853
SPATA5L1
1.000 0.080 15 45406595 intron variant T/A;G snv 4
rs267738
CERS2
1.000 0.040 1 150968149 missense variant T/A;G snv 4.0E-06; 0.15 4
rs4744712
PIP5K1B
1.000 0.080 9 68819791 intron variant A/C;T snv 4
rs7208487
FBXL20
0.925 0.080 17 39387196 intron variant T/A;G snv 4
rs10206899
ALMS1P1
2 73673773 intron variant T/C;G snv 0.21; 3.9E-05 3
rs11123169
PSD4
1.000 0.080 2 113209498 upstream gene variant C/A;T snv 3
rs143193096
IGF1R
15 98916098 missense variant G/A;C snv 8.4E-05; 4.0E-06 3
rs148240484
DPEP1
1.000 0.080 16 89637333 missense variant G/A;C;T snv 5.3E-04; 3.9E-04; 4.0E-06 3
rs16942751
AQP4-AS1
1.000 0.080 18 26813249 intron variant C/A;T snv 3