Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7759295
LOC105375056
1.000 0.040 6 41168112 upstream gene variant C/G;T snv 2
rs9526984
KL
1.000 0.040 13 33035800 intron variant A/G snv 5.5E-02 2
rs398122403
SYNJ1
0.807 0.080 21 32695106 missense variant C/T snv 1.2E-05 11
rs63749806
PSEN1
0.827 0.080 14 73186902 missense variant T/C snv 7
rs1396086494
APP
0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 6
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs17746510
RAPGEF4
0.882 0.080 2 173019562 intron variant T/C;G snv 5
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs16947151
ABI3
0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs1206642175
ESR1
0.925 0.080 6 151808263 synonymous variant G/A snv 7.0E-06 3
rs1372439127
GRN
0.925 0.080 17 44352420 missense variant A/G snv 4.0E-06 3
rs139650807
LRP10
0.925 0.080 14 22875867 missense variant T/A;C snv 6.0E-05 3
rs267606663
APOE
0.925 0.080 19 44909021 missense variant G/A;C snv 7.3E-06 3
rs3763040
AQP4 ; AQP4-AS1
0.925 0.080 18 26864410 intron variant G/A;T snv 3
rs3763043
AQP4 ; AQP4-AS1
0.925 0.080 18 26855854 3 prime UTR variant C/T snv 0.30 3
rs3875089
AQP4 ; AQP4-AS1
0.925 0.080 18 26865469 intron variant T/C snv 0.19 3
rs55781031
BCHE
0.925 0.080 3 165786432 intron variant A/G snv 5.3E-02 3
rs62256378
SUCLG2
0.925 0.080 3 67406609 intron variant G/A;C snv 3
rs6910730
TREM1
0.925 0.080 6 41278895 intron variant A/G snv 0.21 3
rs9877502 0.925 0.080 3 190951729 intergenic variant G/A snv 0.40 3
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 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