Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9904341
BIRC5
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs989692988
TP53
17 7676023 splice donor variant A/C snv 8.0E-06 1
rs9869263
LOC107986170 ; CLDN1
0.925 0.080 3 190312891 synonymous variant A/C;G;T snv 8.0E-06; 0.83; 4.0E-06 3
rs9862
TIMP3 ; SYN3
1.000 0.080 22 32857293 missense variant T/A;C snv 4.0E-06; 0.55 3
rs9856
XIAP
0.925 0.120 X 123911791 3 prime UTR variant C/T snv 0.57 4
rs9836340
EPHA3
3 89356604 intron variant A/G snv 0.33 1
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs975580838
TP63
3 189868592 synonymous variant G/A snv 1
rs975052107
SMIM4 ; PBRM1
3 52563348 missense variant A/G snv 1
rs975030738
MIR483 ; IGF2 ; INS-IGF2
11 2135469 missense variant C/T snv 1
rs974296289
CKAP4
12 106247384 synonymous variant C/T snv 1
rs971586985
CDC73
1.000 0.160 1 193212458 missense variant G/A;T snv 4.0E-06 2.1E-05 3
rs969139366
PDGFRA
4 54277974 missense variant T/C snv 3.5E-05 3
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 9
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 5
rs959969530
ERBB2
17 39727763 missense variant G/A snv 1
rs9589207
MIR17HG ; MIR92A1 ; MIR19B1 ; MIR20A ; MIR19A
0.925 0.080 13 91351335 mature miRNA variant G/A;C snv 5.4E-03; 4.0E-06 4
rs9568036
LPAR6 ; RB1
1.000 0.080 13 48397800 intron variant G/A;T snv 2
rs9533156
TNFSF11
0.807 0.280 13 42573535 intron variant T/C snv 0.47 8
rs9513008
FLT3
13 28053535 intron variant C/T snv 1
rs9503518
SLC22A23 ; PSMG4
6 3273223 synonymous variant A/G snv 8.6E-02 9.0E-02 1
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs942190
TDP1 ; EFCAB11
1.000 0.080 14 89956320 intron variant T/C snv 0.37 2