Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs759304648
GSN
0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 9
rs121909715
GSN
0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 8
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv 8
rs121913547
LYZ
0.807 0.200 12 69350192 missense variant T/C snv 7
rs387906536
LYZ
0.851 0.200 12 69350215 missense variant T/A;C snv 6
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06 5
rs746481995
HSD11B1 ; HSD11B1-AS1
0.882 0.120 1 209707123 missense variant T/C snv 4.0E-06 3
rs121918076
TTR
0.882 0.120 18 31595129 missense variant T/A;C;G snv 3
rs386134269
TTR
0.882 0.120 18 31595127 missense variant A/C;G snv 3
rs146956976
GSN
1.000 0.080 9 121302985 missense variant C/T snv 3.1E-04 4.0E-04 2
rs1363507110
LYZ
1.000 0.080 12 69350201 missense variant T/C snv 1.2E-05 1