Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs55832599
TP53
0.716 0.360 17 7673821 missense variant G/A snv 18
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 17
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv 14
rs1131691003
TP53
0.752 0.360 17 7676381 splice donor variant C/A;G snv 12
rs1131691042
TP53
0.752 0.360 17 7675052 splice donor variant C/T snv 12
rs1057519906
IDH2
0.882 0.120 15 90088607 missense variant T/A;C snv 8
rs28933368
ERBB2 ; MIR4728
0.851 0.080 17 39725721 missense variant G/A snv 5
rs869320686
LZTR1
0.882 22 20990476 missense variant G/A snv 5
rs776893978
LZTR1
22 20997253 missense variant C/T snv 4.4E-05 9.1E-05 1