Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs1364050643
REEP1
0.851 0.240 2 86232711 missense variant G/A snv 5
rs267607102
TARDBP
0.851 0.120 1 11022196 missense variant A/G snv 5
rs587777162
EEF1A2
0.925 0.040 20 63495972 missense variant C/T snv 5
rs80356717
TARDBP
0.851 0.120 1 11018836 missense variant A/G snv 5
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
rs1280914556
KHDRBS1
1 32014269 missense variant A/G snv 2.1E-05 2
rs771884087
LOC105372630 ; SLPI
1.000 0.080 20 45253726 synonymous variant T/C snv 2
rs1457713736
CTSB
8 11850867 stop gained C/T snv 7.0E-06 1
rs374651285
ALB
4 73406645 missense variant G/A snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs756915170
NUP62 ; IL4I1
19 49909654 missense variant T/C snv 4.0E-06 2
rs1467252662
GLRA1 ; LOC112267935
5 151851530 missense variant G/T snv 4.0E-06 2
rs749191312
RBBP9
1.000 0.080 20 18497075 synonymous variant C/T snv 4.0E-06 2
rs121913223
DHFR
1.000 0.040 5 80633904 missense variant T/A snv 4.0E-06 2
rs1805032
CACNB4
1.000 0.040 2 151839238 stop gained G/A snv 4.0E-06 7.0E-06 3
rs62643364
PRNP
0.851 0.160 20 4699466 synonymous variant A/G;T snv 4.0E-06; 1.4E-04 7
rs1471980111
DNAH8
6 38737948 missense variant G/A snv 4.1E-06 7.0E-06 1
rs114925667
NPHP3-ACAD11 ; UBA5
0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs397514662
CUTC ; COX15
0.882 0.120 10 99716419 missense variant A/C;G snv 1.2E-05 4