Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs555607708
CHEK2
0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 17
rs121912678
ACVR1
0.851 0.080 2 157774114 missense variant C/G;T snv 8
rs80359454
BRCA2
0.882 0.200 13 32338828 frameshift variant AAAG/- delins 4
rs149364097
BRIP1
0.925 0.120 17 61801348 missense variant C/A;G;T snv 1.6E-05 3