Disease: Osteosarcoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4148416
ABCC3
0.882 0.040 17 50676062 synonymous variant C/T snv 8.7E-02 0.10 3
rs4150441
ERCC3
0.882 0.040 2 127283339 intron variant T/C snv 0.37 5
rs454006
PRKCG
0.882 0.040 19 53886867 intron variant T/C snv 0.36 3
rs58834075
MIR656
0.882 0.040 14 101066756 non coding transcript exon variant C/G;T snv 4.0E-06; 4.6E-02 3
rs7034162
NFIB
0.882 0.040 9 14190288 intron variant A/T snv 0.81 4
rs756673959
MDM2
0.882 0.040 12 68828867 stop lost T/G snv 3
rs758300152
FSCB
0.882 0.040 14 44504889 missense variant T/C;G snv 1.6E-05; 4.0E-06 3
rs7591996 0.882 0.040 2 6321289 intron variant A/C snv 0.57 3
rs764191858
PDLIM3
0.882 0.040 4 185502359 missense variant G/A snv 3
rs7646409
PIK3CA
0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs770771727
UTRN
0.882 0.040 6 144751941 missense variant A/C;G snv 4.5E-05; 2.5E-05 3
rs779591039
LOC105372630 ; SLPI
0.882 0.040 20 45253712 missense variant G/A snv 3
rs780673045
MDM2
0.882 0.040 12 68839592 missense variant A/G snv 1.2E-05 3
rs8103992 0.882 0.040 19 19554834 regulatory region variant A/C;T snv 3
rs876660254
TP53
0.882 0.040 17 7674963 missense variant G/T snv 4
rs9866361
PIK3CA
0.882 0.040 3 179190061 intron variant G/A snv 0.24 3
rs998074
IGF2R
0.882 0.040 6 160047351 intron variant T/A;C snv 0.53 3
rs998075
IGF2R
0.882 0.040 6 160047246 synonymous variant A/G snv 0.53 0.54 3
rs10019009
DMP1 ; LOC105377323
0.851 0.080 4 87661983 missense variant A/G;T snv 4.0E-06; 0.29 4
rs11866002
CNOT1
0.851 0.120 16 58553833 synonymous variant C/T snv 0.35 0.39 4
rs1215600806
ALPL
0.851 0.120 1 21564100 missense variant T/C snv 1.2E-05 4
rs1233296947
CTNNB1
0.851 0.080 3 41225746 missense variant G/A snv 4.0E-06 5
rs1253660442
SLC19A1
0.851 0.160 21 45531871 missense variant G/A;C snv 4
rs12602273
TP53
0.851 0.080 17 7679695 intron variant C/G snv 0.15 4
rs1416572796
ALPL
0.851 0.120 1 21568170 missense variant G/T snv 4.0E-06 4