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
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs11465996
LY96
0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 7
rs1048719
GM2A
0.925 0.080 5 151253271 missense variant G/A snv 6.1E-02 3.7E-02 2
rs2075783
GM2A
0.925 0.080 5 151267219 3 prime UTR variant A/C snv 0.22 2