Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1566638673
PSEN1
1.000 0.080 14 73186881 inframe insertion -/TAT delins 1
rs63750311
PSEN1
0.790 0.240 14 73192647 missense variant A/C snv 8
rs1362575880
PSEN1
0.851 0.120 14 73192840 missense variant A/C snv 4.0E-06 4
rs63750888
PSEN1
0.925 0.080 14 73192828 missense variant A/C snv 2
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750009
PSEN1
0.851 0.120 14 73192760 missense variant A/C;G snv 5
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs63750590
PSEN1
0.790 0.120 14 73186860 missense variant A/G snv 10
rs63751037
PSEN1
0.790 0.080 14 73173642 missense variant A/G snv 7
rs63751254
PSEN1
0.851 0.160 14 73217210 missense variant A/G snv 4
rs1312532981
PSEN1
1.000 0.080 14 73170846 missense variant A/G snv 1
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
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
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
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
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
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