Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267606673
ATP7A ; PGK1
0.776 0.240 X 78029314 missense variant C/T snv 9
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs901115236
CHCHD10 ; LOC107985577
0.882 0.120 22 23767531 missense variant G/A;T snv 1.5E-05; 1.5E-05 3
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs529782627
APP
0.882 0.120 21 26112051 missense variant C/A snv 4.0E-06 7.0E-06 3
rs533667466
APP
0.925 0.080 21 25911912 missense variant T/C snv 3
rs63750151
APP
0.882 0.080 21 25891761 missense variant C/G;T snv 3
rs8126696 0.882 0.080 21 37358422 intron variant T/C snv 0.64 3
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs74315407
PRNP
0.732 0.240 20 4699848 missense variant G/A snv 8.0E-06 2.1E-05 15
rs74315413
PRNP
0.807 0.160 20 4699780 missense variant A/G snv 8
rs1997794
PDYN-AS1 ; PDYN
0.851 0.120 20 1994212 5 prime UTR variant T/C snv 0.50 4
rs910080
PDYN ; PDYN-AS1
0.851 0.120 20 1979580 3 prime UTR variant A/G snv 0.35 4
rs2235751
PDYN-AS1 ; PDYN
0.882 0.120 20 1989288 intron variant A/G snv 0.40 3
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30