Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1471980111
DNAH8
6 38737948 missense variant G/A snv 4.1E-06 7.0E-06 1
rs374651285
ALB
4 73406645 missense variant G/A snv 1
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs114925667
NPHP3-ACAD11 ; UBA5
0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs398122370
PRNP
0.925 0.160 20 4699851 missense variant G/C snv 4
rs121918413
LOC112267935 ; GLRA1
1.000 0.120 5 151851470 missense variant G/T snv 3
rs1467252662
GLRA1 ; LOC112267935
5 151851530 missense variant G/T snv 4.0E-06 2
rs121913223
DHFR
1.000 0.040 5 80633904 missense variant T/A snv 4.0E-06 2
rs756915170
NUP62 ; IL4I1
19 49909654 missense variant T/C snv 4.0E-06 2
rs771884087
LOC105372630 ; SLPI
1.000 0.080 20 45253726 synonymous variant T/C snv 2
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs141138948
EXOSC3
0.807 0.120 9 37783993 missense variant T/C;G snv 4.1E-04 9