Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs80356726
TARDBP
0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs63750590
PSEN1
0.790 0.120 14 73186860 missense variant A/G snv 10
rs767543900
MAPT
0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8
rs34015634
LRRK2
0.851 0.120 12 40340380 missense variant T/C snv 3.2E-05 1.4E-05 8
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8
rs63750570
MAPT
0.827 0.120 17 46018629 missense variant G/A snv 8
rs63750376
MAPT
0.827 0.120 17 45996657 missense variant G/T snv 7
rs63750416
MAPT
0.851 0.120 17 46010373 missense variant A/C snv 7
rs80356730
TARDBP
0.807 0.120 1 11022418 missense variant A/G snv 8.0E-06 7
rs142444896
CHCHD2
0.807 0.120 7 56106409 missense variant G/A snv 9.3E-03 7.5E-03 6
rs387906711
UBQLN2
0.807 0.120 X 56565389 missense variant C/A;T snv 6.6E-06 6
rs63751068
PSEN1
0.827 0.120 14 73186920 missense variant G/C;T snv 6
rs63751278
PSEN1
0.827 0.120 14 73173631 missense variant A/G snv 6
rs63751294
GRN
0.827 0.120 17 44352404 stop gained C/T snv 8.0E-06 6
rs661
PSEN1
0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 6
rs769446
APOE
0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02 6
rs775129479
SPSB3 ; IGFALS
0.851 0.120 16 1791387 missense variant G/A;C;T snv 1.6E-05; 8.1E-06; 8.1E-06 6
rs781587642
TUBA4A ; STK16
0.851 0.120 2 219250557 missense variant G/A;C snv 2.0E-05 6
rs80356715
TARDBP
0.807 0.120 1 11016874 missense variant C/G;T snv 8.0E-06; 2.2E-04 6