Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518919
PSEN1
0.851 0.120 14 73171023 missense variant T/G snv 5
rs63750050
PSEN1
0.925 0.080 14 73198106 missense variant T/G snv 5
rs63749961
PSEN1
0.925 0.080 14 73192772 missense variant T/G snv 3
rs63751071
PSEN1
1.000 0.080 14 73173656 missense variant T/G snv 1
rs63750599
PSEN1
0.827 0.160 14 73170963 missense variant T/C snv 7
rs63751163
PSEN1
0.807 0.120 14 73192844 missense variant T/C snv 7
rs63751024
PSEN1
0.851 0.120 14 73192793 missense variant T/C snv 4
rs866914724
PSEN1
0.882 0.080 14 73173685 missense variant T/C snv 3
rs906454643
PSEN1
0.882 0.080 14 73217219 missense variant T/C snv 4.0E-06 3
rs3025786
PSEN1
1.000 0.080 14 73198010 non coding transcript exon variant T/C snv 3.5E-02 3.6E-02 1
rs63750265
PSEN1
0.882 0.080 14 73186869 missense variant T/A;C;G snv 3
rs63751106
PSEN1
0.827 0.080 14 73173643 missense variant T/A;C snv 5
rs63750004
PSEN1
0.851 0.080 14 73173655 missense variant T/A;C snv 4
rs765670175
PSEN1
0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 7
rs63750929
PSEN1
0.882 0.080 14 73217177 missense variant G/T snv 4
rs63750815
PSEN1
0.882 0.080 14 73170974 missense variant G/T snv 3
rs1566656702
PSEN1
1.000 0.080 14 73217173 missense variant G/T snv 1
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs63750646
PSEN1
0.807 0.120 14 73217147 missense variant G/C snv 6
rs63751223
PSEN1
0.807 0.160 14 73219161 missense variant G/C snv 6
rs63751141
PSEN1
0.882 0.080 14 73170984 missense variant G/C snv 3
rs63750852
PSEN1
0.790 0.120 14 73170998 missense variant G/A;T snv 8
rs661
PSEN1
0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 6
rs165932
PSEN1
0.925 0.080 14 73198145 intron variant G/A;T snv 0.61 2
rs63750219
PSEN1
1.000 0.080 14 73206385 splice acceptor variant G/A;T snv 1