Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750391
PSEN1
0.882 0.160 14 73173665 missense variant G/A;C;T snv 3
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
rs63750577
PSEN1
0.827 0.120 14 73186881 missense variant C/T snv 8
rs63750301
PSEN1
0.827 0.120 14 73198052 missense variant C/T snv 4.0E-06 6
rs63750730
PSEN1
0.827 0.120 14 73173574 missense variant C/T snv 6
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
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8
rs63749805
PSEN1
0.807 0.120 14 73173577 missense variant C/G;T snv 6
rs63750886
PSEN1
0.851 0.080 14 73198072 missense variant C/G snv 5
rs41345849
PSEN1
1.000 0.080 14 73173634 missense variant C/G snv 1
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs1446915570
PSEN1
0.925 0.080 14 73173623 synonymous variant A/T snv 4.0E-06 7.0E-06 2
rs779296437
PSEN1
0.925 0.080 14 73192699 missense variant A/T snv 4.0E-06 2
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs63750353
PSEN1
0.925 0.080 14 73173630 missense variant A/G;T snv 2