Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 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
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 16
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs1569151872
TSPEAR-AS1 ; TSPEAR
0.851 0.240 21 44509225 frameshift variant GAC/AA delins 14
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 11
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs876660634
PTEN
0.807 0.200 10 87925551 missense variant A/C;G snv 10
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9