Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998075
IGF2R
0.882 0.040 6 160047246 synonymous variant A/G snv 0.53 0.54 3
rs998074
IGF2R
0.882 0.040 6 160047351 intron variant T/A;C snv 0.53 3
rs9895829
TP53
0.807 0.080 17 7675361 5 prime UTR variant A/G snv 7.4E-02 6
rs9866361
PIK3CA
0.882 0.040 3 179190061 intron variant G/A snv 0.24 3
rs886041906
CTLA4
0.882 0.200 2 203868002 stop gained G/A snv 6
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876660254
TP53
0.882 0.040 17 7674963 missense variant G/T snv 4
rs863223301
TP53
0.925 0.080 17 7675130 frameshift variant -/CCATGGC delins 2
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs820196
SMIM5 ; RECQL5
0.807 0.160 17 75631459 missense variant T/A;C snv 1.6E-05; 0.26 6
rs8103992 0.882 0.040 19 19554834 regulatory region variant A/C;T snv 3
rs8103851
PRKCG
0.851 0.040 19 53894400 intron variant C/G snv 0.44 5
rs8064946
TP53 ; WRAP53
0.851 0.080 17 7685993 non coding transcript exon variant G/C snv 0.32 4
rs7958904
HOTAIR
0.724 0.200 12 53963768 non coding transcript exon variant C/A;G snv 15
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs780673045
MDM2
0.882 0.040 12 68839592 missense variant A/G snv 1.2E-05 3
rs779591039
LOC105372630 ; SLPI
0.882 0.040 20 45253712 missense variant G/A snv 3
rs770771727
UTRN
0.882 0.040 6 144751941 missense variant A/C;G snv 4.5E-05; 2.5E-05 3
rs7646409
PIK3CA
0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs764191858
PDLIM3
0.882 0.040 4 185502359 missense variant G/A snv 3
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs763098116
TP53
0.925 0.040 17 7673790 missense variant C/A;T snv 4.0E-06 3
rs7591996 0.882 0.040 2 6321289 intron variant A/C snv 0.57 3
rs758300152
FSCB
0.882 0.040 14 44504889 missense variant T/C;G snv 1.6E-05; 4.0E-06 3
rs756673959
MDM2
0.882 0.040 12 68828867 stop lost T/G snv 3