Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs63750590
PSEN1
0.790 0.120 14 73186860 missense variant A/G snv 10
rs63750900
PSEN1
0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 9
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8
rs63750311
PSEN1
0.790 0.240 14 73192647 missense variant A/C snv 8
rs63750577
PSEN1
0.827 0.120 14 73186881 missense variant C/T snv 8
rs63750852
PSEN1
0.790 0.120 14 73170998 missense variant G/A;T snv 8
rs63750599
PSEN1
0.827 0.160 14 73170963 missense variant T/C snv 7
rs63751037
PSEN1
0.790 0.080 14 73173642 missense variant A/G snv 7
rs63751163
PSEN1
0.807 0.120 14 73192844 missense variant T/C snv 7
rs765670175
PSEN1
0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 7
rs63749805
PSEN1
0.807 0.120 14 73173577 missense variant C/G;T snv 6
rs63750301
PSEN1
0.827 0.120 14 73198052 missense variant C/T snv 4.0E-06 6
rs63750646
PSEN1
0.807 0.120 14 73217147 missense variant G/C snv 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
rs63751223
PSEN1
0.807 0.160 14 73219161 missense variant G/C snv 6
rs661
PSEN1
0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 6
rs1057518919
PSEN1
0.851 0.120 14 73171023 missense variant T/G snv 5