Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs372392424
PIGG
0.882 0.240 4 523849 missense variant C/T snv 6.7E-05 7.7E-05 8
rs1085308045
PTEN
0.807 0.160 10 87933128 missense variant C/G;T snv 8
rs1085308056
PTEN
0.851 0.160 10 87957850 splice region variant C/G snv 8
rs1554893835
PTEN
0.827 0.240 10 87894110 splice donor variant G/C;T snv 8
rs755246809
AHI1
0.827 0.280 6 135404951 frameshift variant T/- delins 5.9E-04 4.9E-05 7
rs1057524237
COL11A1
0.851 0.280 1 102915626 splice region variant C/T snv 7
rs1085308050
PTEN
0.827 0.160 10 87933178 frameshift variant -/A delins 7
rs1085308054
PTEN
0.827 0.160 10 87952231 frameshift variant AT/- delins 7
rs869312713
ANKRD11
0.882 0.320 16 89280070 stop gained C/A snv 6
rs1554943158
DEAF1
0.882 0.040 11 681045 inframe deletion CTT/- delins 6
rs886039903
FGF12
0.807 0.200 3 192335434 missense variant C/T snv 6
rs878853165
HOOK2 ; MAST1
0.882 0.200 19 12843558 missense variant C/T snv 6
rs1085308048
PTEN
0.851 0.320 10 87933175 stop gained T/G snv 6
rs1085308051
PTEN
0.882 0.200 10 87933229 missense variant A/G snv 4.0E-06 6
rs1085308047
PTEN ; KLLN
0.827 0.160 10 87864509 missense variant A/G snv 6
rs1554297905
RALA
0.882 0.160 7 39686740 missense variant G/A snv 6
rs752134549
RSRC2
0.827 0.200 12 122517404 missense variant C/T snv 1.6E-05 7.0E-06 6
rs879253767
SCN2A
0.882 0.080 2 165313738 frameshift variant T/- delins 6
rs869312696
ASXL3
0.882 0.160 18 33739086 stop gained C/A snv 5
rs1564365418
GRIN1
0.882 0.120 9 137163846 missense variant G/T snv 5
rs869312686
HCFC1
0.882 0.120 X 153952053 missense variant G/C;T snv 5
rs1414334
HTR2C
0.851 0.160 X 114903581 intron variant C/G snv 5
rs869312671
MTOR ; MTOR-AS1
0.882 0.160 1 11144735 missense variant C/T snv 5
rs1085308052
PTEN
0.851 0.160 10 87952144 frameshift variant -/T delins 5
rs1085308044
PTEN ; KLLN
0.882 0.120 10 87864504 missense variant A/C snv 5