Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1353759920
TP73
0.851 0.120 1 3707593 missense variant C/A snv 2.1E-05 4
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
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 28
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs3749474
TMEM165 ; CLOCK
0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs1979277
SHMT1
0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv 8
rs1057519952
RHOA
0.882 0.160 3 49375577 missense variant G/A snv 5
rs1057519954
RHOA
0.882 0.160 3 49375465 missense variant T/A;C;G snv 4
rs121908689
RAD54L ; LRRC41
0.925 0.120 1 46272758 missense variant T/A snv 2
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs760228510
PMS2
0.925 0.240 7 5999182 stop gained G/A;C snv 6
rs1057519942
PIK3CA
0.724 0.320 3 179203760 missense variant G/A snv 16