Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1562846694
ACTL6B ; TFR2
0.763 0.320 7 100643252 inframe deletion TTCGCTCCACGCACT/- delins 32
rs1445081098
COMT ; MIR4761
0.724 0.480 22 19963746 missense variant G/C snv 4.0E-06 17
rs367543041
TARDBP
0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs431905504
SLC6A3
0.776 0.280 5 1411242 splice donor variant C/T snv 6.4E-06 9
rs11538758
PRNP
0.882 0.160 20 4699534 missense variant C/A;T snv 8
rs199935023
PLA2G6
0.882 0.040 22 38132917 missense variant C/A;T snv 4.9E-05; 3.6E-05 4
rs63750929
PSEN1
0.882 0.080 14 73217177 missense variant G/T snv 4