Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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 213
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 25
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 21
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs1800371
TP53
0.742 0.240 17 7676230 missense variant G/A;T snv 1.2E-03 15
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 14
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10 8
rs55832599
TP53
0.716 0.360 17 7673821 missense variant G/A snv 5
rs1064795841
TP53
0.882 0.080 17 7674971 missense variant C/T snv 4
rs1131691029
TP53
0.827 0.160 17 7673794 missense variant C/G snv 4
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 4
rs1427471466
TP53
1.000 0.080 17 7674183 frameshift variant G/- delins 1
rs746504075
TP53
1.000 0.080 17 7674290 missense variant C/G;T snv 4.0E-06 1