Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs796052243
SPATA5
0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs28936415
PMM2
0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs1555706928
SETBP1
0.851 0.240 18 44951954 missense variant G/A snv 8
rs363050
SNAP25-AS1 ; SNAP25
0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs878853322
PPT1
0.925 0.160 1 40078573 missense variant G/A snv 4
rs1133174
SORL1
0.882 0.120 11 121631046 3 prime UTR variant G/A snv 0.55 3
rs9637454
KCNMB2 ; KCNMB2-AS1
0.882 0.120 3 178539774 intron variant G/A snv 0.23 3
rs2298813
SORL1
0.790 0.120 11 121522975 missense variant G/A;T snv 7.2E-02; 4.0E-06 7
rs796052019
PCCA
0.882 0.160 13 100157297 missense variant G/A;T snv 4.0E-06 3
rs1193124736
APP
0.851 0.120 21 25982462 missense variant G/T snv 7.0E-06 4
rs139632595
EXOSC9
0.807 0.160 4 121801465 missense variant T/C snv 6.0E-05 2.5E-04 19
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs7127507
BDNF-AS ; BDNF
0.827 0.080 11 27693337 intron variant T/C snv 0.34 6
rs73069071
IAPP ; SLCO1A2
0.807 0.240 12 21357370 intron variant T/C snv 0.14 6
rs7354779
DNMT3L ; DNMT3L-AS1
0.827 0.200 21 44250887 missense variant T/C snv 0.21 6
rs10761482
ANK3
0.851 0.120 10 60325579 intron variant T/C snv 0.70 4
rs4935774
LOC105369536 ; SORL1
0.925 0.080 11 121451045 intron variant T/C snv 0.32 2
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs864309505
TPP1
0.807 0.200 11 6615220 missense variant T/G snv 10