Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1312532981
PSEN1
1.000 0.080 14 73170846 missense variant A/G snv 1
rs1566630910
PSEN1
1.000 0.080 14 73173651 missense variant G/A snv 1
rs1566638673
PSEN1
1.000 0.080 14 73186881 inframe insertion -/TAT delins 1
rs1566656702
PSEN1
1.000 0.080 14 73217173 missense variant G/T snv 1
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
rs3025786
PSEN1
1.000 0.080 14 73198010 non coding transcript exon variant T/C snv 3.5E-02 3.6E-02 1
rs41345849
PSEN1
1.000 0.080 14 73173634 missense variant C/G snv 1
rs63750219
PSEN1
1.000 0.080 14 73206385 splice acceptor variant G/A;T snv 1
rs63751071
PSEN1
1.000 0.080 14 73173656 missense variant T/G snv 1
rs1446915570
PSEN1
0.925 0.080 14 73173623 synonymous variant A/T snv 4.0E-06 7.0E-06 2
rs165932
PSEN1
0.925 0.080 14 73198145 intron variant G/A;T snv 0.61 2
rs200576075
PSEN1
0.925 0.080 14 73171031 missense variant C/T snv 2
rs63750353
PSEN1
0.925 0.080 14 73173630 missense variant A/G;T snv 2
rs63750888
PSEN1
0.925 0.080 14 73192828 missense variant A/C snv 2
rs779296437
PSEN1
0.925 0.080 14 73192699 missense variant A/T snv 4.0E-06 2
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
rs63749961
PSEN1
0.925 0.080 14 73192772 missense variant T/G snv 3
rs63750265
PSEN1
0.882 0.080 14 73186869 missense variant T/A;C;G snv 3
rs63750391
PSEN1
0.882 0.160 14 73173665 missense variant G/A;C;T snv 3
rs63750800
PSEN1
0.882 0.080 14 73173585 missense variant G/A snv 3
rs63750815
PSEN1
0.882 0.080 14 73170974 missense variant G/T snv 3
rs63751141
PSEN1
0.882 0.080 14 73170984 missense variant G/C snv 3
rs866914724
PSEN1
0.882 0.080 14 73173685 missense variant T/C snv 3