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
rs3743930
MEFV
0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs28940578
MEFV
0.716 0.400 16 3243405 missense variant C/T snv 1.4E-04 6.3E-05 16
rs398122820
B2M
0.790 0.240 15 44715641 missense variant G/A snv 8
rs121918098
TTR
0.807 0.200 18 31592939 missense variant A/G snv 7
rs121909612
FGA
0.807 0.160 4 154585795 missense variant T/A snv 4.0E-06 7.0E-06 6
rs920832709
GSN
0.851 0.200 9 121321384 synonymous variant G/T snv 4
rs121918093
TTR
0.882 0.200 18 31592944 missense variant G/A;C snv 4.0E-06 4
rs201564694
APCS
0.882 0.120 1 159588626 missense variant T/C snv 3
rs753950237
DPYD
0.882 0.160 1 97082400 missense variant G/A snv 4.0E-06 7.0E-06 3