Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs267606670
ATP1A3
0.790 0.320 19 41968837 missense variant C/A;T snv 19
rs587784105
NSD1
0.732 0.440 5 177235863 stop gained G/A snv 19
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs1566823361
FGF14
0.742 0.440 13 101726732 frameshift variant -/G delins 18
rs28935468
MECP2
0.732 0.240 X 154030912 missense variant G/A snv 17
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs797044849
GRIN2B
0.807 0.160 12 13567164 missense variant C/A;G;T snv 4.0E-06 17
rs80356537
ATP1A3
0.752 0.320 19 41970405 missense variant C/A;G;T snv 17
rs1057518907
GNAS
0.732 0.320 20 58891811 stop gained C/G;T snv 16
rs587777630
STAT1
0.716 0.440 2 190986921 missense variant G/A snv 16
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs1569151872
TSPEAR-AS1 ; TSPEAR
0.851 0.240 21 44509225 frameshift variant GAC/AA delins 14
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
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs398122403
SYNJ1
0.807 0.080 21 32695106 missense variant C/T snv 1.2E-05 11
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs2230199
C3
0.763 0.240 19 6718376 missense variant G/C;T snv 0.15 10
rs28936379
PSEN2
0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 10
rs876660634
PTEN
0.807 0.200 10 87925551 missense variant A/C;G snv 10