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
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs1044250
ANGPTL4
0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs121918094
TTR
0.827 0.280 18 31592921 missense variant T/C snv 8
rs1040441824
PTS
0.882 0.200 11 112233502 missense variant A/G snv 2.1E-05 4