Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750687
PSEN1
0.752 0.200 14 73217137 missense variant C/A;G;T snv 30
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 29
rs61752717
MEFV
0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 20
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 5
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 5
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 5
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 4
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 4
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 4
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 3
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 3
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 2
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 2
rs63750399
APP
0.882 0.080 21 25891787 missense variant T/A;C snv 2
rs63750734
APP
0.851 0.080 21 25891790 missense variant C/T snv 2
rs63750921
APP
0.882 0.200 21 25891820 missense variant G/C snv 2
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs74315408
PRNP
0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 2
rs1057518919
PSEN1
0.851 0.120 14 73171023 missense variant T/G snv 2
rs63749891
PSEN1
0.851 0.080 14 73198094 missense variant G/C;T snv 2
rs63750009
PSEN1
0.851 0.120 14 73192760 missense variant A/C;G snv 2
rs63750599
PSEN1
0.827 0.160 14 73170963 missense variant T/C snv 2
rs63751122
APP
0.925 0.080 21 25891765 missense variant A/G snv 1
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 1
rs121917808
PSEN1
0.882 0.080 14 73219192 missense variant C/A snv 1