Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs749203329
MLLT1
0.882 0.080 19 6213787 missense variant C/T snv 2.0E-05 1.4E-05 7
rs869320624
EMC1-AS1 ; EMC1
0.776 0.400 1 19220814 frameshift variant AAGG/- delins 1.4E-05 13
rs769236847
CZ1P-ASNS ; ASNS
0.807 0.200 7 97869011 missense variant C/T snv 4.0E-06 3.5E-05 8
rs146539065
SEPSECS
0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05 34
rs776969714
SEPSECS
0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 34
rs139632595
EXOSC9
0.807 0.160 4 121801465 missense variant T/C snv 6.0E-05 2.5E-04 19
rs28936415
PMM2
0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs73069071
IAPP ; SLCO1A2
0.807 0.240 12 21357370 intron variant T/C snv 0.14 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs9637454
KCNMB2 ; KCNMB2-AS1
0.882 0.120 3 178539774 intron variant G/A snv 0.23 3
rs4935774
LOC105369536 ; SORL1
0.925 0.080 11 121451045 intron variant T/C snv 0.32 2
rs7127507
BDNF-AS ; BDNF
0.827 0.080 11 27693337 intron variant T/C snv 0.34 6
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs1133174
SORL1
0.882 0.120 11 121631046 3 prime UTR variant G/A snv 0.55 3
rs704180
ABCC9
0.807 0.240 12 21841177 intron variant A/G snv 0.55 6
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
rs10761482
ANK3
0.851 0.120 10 60325579 intron variant T/C snv 0.70 4