Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs397514662
CUTC ; COX15
0.882 0.120 10 99716419 missense variant A/C;G snv 1.2E-05 4
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
rs74315322
HAX1
1.000 0.040 1 154275165 stop gained C/T snv 3.6E-05 3
rs121913223
DHFR
1.000 0.040 5 80633904 missense variant T/A 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
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
rs374651285
ALB
4 73406645 missense variant G/A snv 1