Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs587781858
TP53
0.742 0.360 17 7669671 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 12
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs1288373809
TP53
0.882 0.120 17 7673255 synonymous variant G/A snv 5.3E-06 5
rs1177881399
TP53
0.925 0.080 17 7673557 missense variant T/C snv 4.0E-06 2
rs1159579789
TP53
0.925 0.080 17 7673578 missense variant T/C snv 4.0E-06 3
rs1457582183
TP53
0.827 0.200 17 7673608 missense variant G/A;C snv 7.0E-06 5
rs55819519
TP53
0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs1064795369
TP53
0.882 0.080 17 7673791 missense variant A/C;G snv 3
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs587781433
TP53
0.925 0.080 17 7674197 missense variant T/C;G snv 3
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs1064794312
TP53
0.925 0.080 17 7674278 missense variant A/G snv 8.0E-06 2
rs1625895
TP53
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1800372
TP53
0.752 0.240 17 7674892 synonymous variant T/A;C snv 1.3E-02 15
rs397516435
TP53
0.851 0.280 17 7674945 stop gained G/A;C snv 4.0E-06 6
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32