Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750635
MAPT
0.851 0.120 17 46014286 missense variant C/T snv 5
rs63750959
MAPT
0.827 0.200 17 45962351 missense variant G/A;T snv 6.0E-05 5
rs1235948930
MAPT
0.882 0.120 17 45983865 missense variant C/T snv 7.0E-06 4
rs63750129
MAPT
0.882 0.120 17 45996612 missense variant A/C snv 4.0E-06 4
rs1182182524
MAPT
0.882 0.120 17 45983724 missense variant T/G snv 1.4E-05 3
rs63750573
MAPT
0.882 0.120 17 46018627 missense variant A/G snv 3
rs63750905
MAPT
0.882 0.120 17 46018624 missense variant G/T snv 3
rs63751165
MAPT
0.925 0.120 17 46010401 missense variant G/A;T snv 3
rs760049824
MAPT
0.882 0.120 17 45983867 missense variant T/A;C snv 4.2E-06; 8.5E-06 3
rs1012826460
MAPT
0.925 0.120 17 45971888 missense variant G/A snv 4.0E-06 1.4E-05 2
rs1295855402
MAPT
0.925 0.120 17 46024034 missense variant C/T snv 7.0E-06 2
rs63750711
MAPT
0.925 0.120 17 46018645 missense variant A/T snv 2
rs63751264
MAPT
0.925 0.120 17 46018726 missense variant A/T snv 2
rs751739883
MAPT
0.925 0.120 17 45983891 missense variant C/T snv 4.4E-06 2
rs774890160
MAPT
0.925 0.120 17 45974388 missense variant T/C snv 4.2E-06 2
rs1804469
MSMB ; LOC105378287
0.925 0.120 10 46033495 missense variant T/C snv 2
rs747481280
OPTN
0.851 0.120 10 13132068 missense variant T/G snv 8.0E-06 4
rs139108915
PAX5
0.925 0.120 9 36840599 missense variant G/A snv 1.0E-05 9.8E-05 3
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs747019990
PRNP
0.851 0.120 20 4699336 missense variant C/T snv 3.6E-05 7.0E-06 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
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