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
rs999036825
AP1M1
1.000 0.080 19 16228789 missense variant G/A snv 2.1E-05 1
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
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs995629797
PALB2
1.000 0.080 16 23626254 stop gained A/T snv 8.0E-06 2.8E-05 2
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
rs991177157
FBXW7
1.000 0.080 4 152411455 missense variant C/T snv 1
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
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
rs981782
HCN1
0.851 0.080 5 45285616 intron variant A/C snv 0.34 4
rs981042
CDKAL1
0.925 0.080 6 20535303 intron variant G/T snv 0.10 2
rs9790517
TET2
0.925 0.080 4 105163621 intron variant C/T snv 0.20 2
rs975263
MACC1
0.827 0.120 7 20158817 stop gained G/A;T snv 0.34 7
rs974334
GPX6
0.925 0.080 6 28506441 intron variant C/G snv 0.26 0.29 2