Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs55819519
TP53
0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 21
rs4245739
MDM4
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 21
rs799917
BRCA1
0.708 0.320 17 43092919 missense variant G/A;C;T snv 0.40; 1.6E-05 18
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs121913243
MET
0.827 0.160 7 116777410 missense variant A/C;G snv 1.2E-05 7
rs1284110310
ERBB2
0.882 0.200 17 39706999 missense variant G/A snv 7.0E-06 5
rs372032595
DLD
0.925 0.080 7 107904960 missense variant T/G snv 4.0E-06 3
rs1374154597
PPP2R3A
1.000 0.120 3 136023097 frameshift variant -/G delins 2
rs746354996
SNAPC5 ; MAP2K1
15 66489734 missense variant G/A snv 2.8E-05 7.0E-06 1