Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs869025608
MAP2K1
0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs80359306
BRCA2
0.827 0.280 13 32333284 frameshift variant A/-;AA delins 6
rs80357522
BRCA1
0.776 0.280 17 43093570 frameshift variant TTTT/-;TT;TTT;TTTTT delins 7.0E-06 10
rs760228510
PMS2
0.925 0.240 7 5999182 stop gained G/A;C snv 6
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs756091827
MYC ; CASC11
0.851 0.200 8 127738435 missense variant C/G;T snv 6
rs750664148
CASC11 ; MYC
0.851 0.200 8 127738434 missense variant A/C;G snv 5
rs75002266
ORC4
0.827 0.160 2 147939241 missense variant G/A snv 3.2E-03 3.0E-03 6
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs63750042
MSH2
0.925 0.240 2 47408415 stop gained C/G;T snv 4.0E-06 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs4245739
MDM4
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 21
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs398122820
B2M
0.790 0.240 15 44715641 missense variant G/A snv 8
rs398122800
CASP10
1.000 0.120 2 201209189 frameshift variant -/A ins 1
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs3749474
TMEM165 ; CLOCK
0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs34767364
NBN
0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 20