Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750311
PSEN1
0.790 0.240 14 73192647 missense variant A/C snv 8
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 4
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs28936379
PSEN2
0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs1712572
LINC00882
1.000 0.080 3 106898231 non coding transcript exon variant A/C;G;T snv 1
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
rs115865530
PSEN1
0.925 0.080 14 73206449 missense variant A/G snv 1.4E-04 4.2E-05 2
rs1015909000
NFIB
1.000 0.080 9 14146790 missense variant A/G snv 1
rs1393704451
RANBP2 ; SH3RF3 ; SH3RF3-AS1
1.000 0.080 2 109129746 missense variant A/G snv 1
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
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
rs121917808
PSEN1
0.882 0.080 14 73219192 missense variant C/A snv 3
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 10
rs63751235
PSEN1
0.807 0.120 14 73198117 missense variant C/G snv 6
rs63750363
APP
1.000 0.080 21 25897642 missense variant C/G snv 1.2E-05 7.0E-06 1
rs773029808
SORBS2
1.000 0.080 4 185626897 missense variant C/G snv 2.0E-05 1
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
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