Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11931074
SNCA ; LOC105377329
0.851 0.080 4 89718364 intron variant G/A;C;T snv 7
rs63750802
PSEN1
0.851 0.080 14 73219144 missense variant T/G snv 7
rs63751032
PSEN1
0.851 0.080 14 73219156 missense variant T/A;G snv 7
rs63751037
PSEN1
0.790 0.080 14 73173642 missense variant A/G snv 7
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs201106962
SNCA
0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 5
rs2306604
TFAM
0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs28936380
PSEN2
0.827 0.080 1 226885546 missense variant C/G;T snv 1.2E-05 5
rs63749835
PSEN1
0.851 0.080 14 73192799 missense variant T/C snv 5
rs1801474
PRKN
0.851 0.080 6 162201165 missense variant C/T snv 7.1E-02 5.3E-02 4
rs2281983
PITX3
0.851 0.080 10 102231624 missense variant G/A;C;T snv 0.62; 8.3E-06 4
rs571825723
PSEN1
0.925 0.080 14 73211867 missense variant C/T snv 4.4E-05 2.8E-05 4
rs6332
NTF3
0.851 0.080 12 5494466 synonymous variant G/A;T snv 0.49; 3.2E-05 4
rs6347
SLC6A3
0.851 0.080 5 1411297 synonymous variant T/C snv 0.23 0.32 4
rs63750004
PSEN1
0.851 0.080 14 73173655 missense variant T/A;C snv 4
rs763872192
CD36
0.882 0.080 7 80672000 missense variant C/T snv 2.8E-05 4
rs9331896
CLU ; MIR6843
0.851 0.080 8 27610169 intron variant C/G;T snv 4
rs9357347
LOC107986595
0.851 0.080 6 41182853 intergenic variant A/C;T snv 4
rs1010159
SORL1
0.882 0.080 11 121612692 non coding transcript exon variant C/T snv 0.55 0.55 3
rs1043202
SMUG1
0.882 0.080 12 54182178 missense variant T/A snv 3
rs1341026713
APP
0.925 0.080 21 25955719 missense variant G/A snv 4.0E-06 1.4E-05 3
rs142690225
PSEN2
0.925 0.080 1 226894111 missense variant G/A snv 1.1E-04 1.1E-04 3
rs2420616
GRK5
0.882 0.080 10 119316984 intron variant A/G snv 0.69 3
rs2618516
SPON1
0.882 0.080 11 14000092 intron variant T/C snv 0.65 3
rs4752293
GRK5
0.882 0.080 10 119342186 intron variant C/T snv 0.74 3