Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs121912665
TP53
1.000 0.120 17 7674965 missense variant G/A snv 2.4E-05 7.0E-06 7
rs764803020
TP53
0.851 0.040 17 7673750 frameshift variant -/TTTCCGCCGG delins 4.0E-06 5
rs779196500
TP53
0.882 0.120 17 7675187 missense variant G/A snv 4.0E-06 5
rs781490101
TP53
0.851 0.040 17 7673748 missense variant T/C snv 8.0E-06 5
rs863224683
TP53
17 7675224 missense variant G/A;C snv 4
rs573154688
TP53
1.000 0.160 17 7670711 missense variant C/T snv 4.4E-05 3.5E-05 3
rs863224682
TP53
1.000 0.080 17 7669655 missense variant C/A;T snv 4.0E-06 2
rs771939956
TP53
17 7670705 missense variant C/T snv 4.0E-06 7.0E-06 1
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1259653415
TFRC
1.000 0.080 3 196071416 missense variant T/C snv 7.0E-06 3
rs7726159
TERT
0.790 0.160 5 1282204 intron variant C/A snv 0.29 10