Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs999737
RAD51B
0.776 0.200 14 68567965 intron variant C/T snv 0.16 8
rs9989661
LMTK3
0.925 0.080 19 48510834 intron variant T/C snv 0.21 2
rs997669
CCNE1
0.925 0.080 19 29813576 intron variant T/C snv 0.30 2
rs9959491 1.000 0.080 18 27826891 intergenic variant C/T snv 0.61 1
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs9954058
SETBP1
1.000 0.080 18 44831838 intron variant G/A;C snv 1
rs9952980
SLC14A2
1.000 0.080 18 45308832 intron variant T/A;C snv 1
rs9940645
ZNF423
0.925 0.080 16 49797677 intron variant A/G snv 0.54 2
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9913477
BAIAP2
0.925 0.080 17 81041898 intron variant A/C;G snv 2
rs9904341
BIRC5
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs9900506
RPTOR
0.925 0.080 17 80648576 intron variant G/A snv 0.59 2
rs989902
PTPN13
0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53 12
rs9888739
ITGAM
0.882 0.120 16 31301932 intron variant C/T snv 0.26 3
rs9884765 1.000 0.080 4 91717049 intergenic variant T/A;C snv 1
rs9879992
GSK3B
0.882 0.120 3 119993874 intron variant A/G snv 0.28 4
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 7
rs9874
SELENOS
0.925 0.080 15 101271199 3 prime UTR variant T/C snv 0.23 2
rs985325188
APEX1 ; OSGEP
0.851 0.080 14 20456806 missense variant A/C snv 4
rs984257990
INS-IGF2 ; IGF2 ; MIR483
0.925 0.080 11 2135495 missense variant A/G snv 4.0E-06 7.0E-06 3
rs9839776
SOX2-OT
0.851 0.160 3 181593779 intron variant C/G;T snv 4
rs9837602
FILIP1L ; CMSS1
1.000 0.080 3 100105841 intron variant G/A snv 0.18 1
rs9834244 0.776 0.120 3 151704793 intergenic variant G/A snv 6.1E-02 10
rs9833888
CMSS1 ; FILIP1L
1.000 0.080 3 100004736 intron variant G/T snv 0.18 1
rs981782
HCN1
0.851 0.080 5 45285616 intron variant A/C snv 0.34 4