Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 2