Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750907
PSEN1
0.807 0.120 14 73173667 missense variant C/T snv 6
rs63750001
PSEN1
0.851 0.080 14 73219188 missense variant C/T snv 4
rs63749885
PSEN1
0.882 0.080 14 73186859 missense variant C/T snv 3
rs63749925
PSEN1
0.882 0.080 14 73219191 missense variant C/T snv 3
rs200576075
PSEN1
0.925 0.080 14 73171031 missense variant C/T snv 2
rs1566657804
PSEN1
1.000 0.080 14 73219182 missense variant C/T snv 1
rs1800839
PSEN1
1.000 0.080 14 73136423 5 prime UTR variant C/T snv 5.7E-02 1
rs63750900
PSEN1
0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 9
rs63750444
PSEN1
0.882 0.080 14 73192745 missense variant G/A snv 4
rs63750800
PSEN1
0.882 0.080 14 73173585 missense variant G/A snv 3
rs1566630910
PSEN1
1.000 0.080 14 73173651 missense variant G/A snv 1
rs63750391
PSEN1
0.882 0.160 14 73173665 missense variant G/A;C;T 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
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
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
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
rs765670175
PSEN1
0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 7
rs63751106
PSEN1
0.827 0.080 14 73173643 missense variant T/A;C snv 5