Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs63750687
PSEN1
0.752 0.200 14 73217137 missense variant C/A;G;T snv 33
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
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
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
rs63750522
PSEN1
0.827 0.120 14 73173644 missense variant G/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
rs1051338
LIPA
0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 7