Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1043679457
ERCC8
0.752 0.400 5 60927745 intron variant C/A;G;T snv 33
rs1057516264
TPP1
0.776 0.280 11 6614968 frameshift variant C/-;CC delins 13
rs10761482
ANK3
0.851 0.120 10 60325579 intron variant T/C snv 0.70 4
rs1133174
SORL1
0.882 0.120 11 121631046 3 prime UTR variant G/A snv 0.55 3
rs1193124736
APP
0.851 0.120 21 25982462 missense variant G/T snv 7.0E-06 4
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs139632595
EXOSC9
0.807 0.160 4 121801465 missense variant T/C snv 6.0E-05 2.5E-04 19
rs146539065
SEPSECS
0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05 34
rs1554901898
TPP1
0.776 0.280 11 6616858 frameshift variant A/- delins 12
rs1554902217
TPP1
0.851 0.160 11 6618821 frameshift variant A/- del 7
rs1555642784
CNTNAP1
0.851 0.160 17 42688979 frameshift variant -/C delins 5
rs1555706928
SETBP1
0.851 0.240 18 44951954 missense variant G/A snv 8
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs2298813
SORL1
0.790 0.120 11 121522975 missense variant G/A;T snv 7.2E-02; 4.0E-06 7
rs28936415
PMM2
0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs363050
SNAP25-AS1 ; SNAP25
0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs4935774
LOC105369536 ; SORL1
0.925 0.080 11 121451045 intron variant T/C snv 0.32 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs672601366
KIF1A
0.851 0.120 2 240786339 missense variant C/G snv 6
rs704180
ABCC9
0.807 0.240 12 21841177 intron variant A/G snv 0.55 6
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