Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs7127507
BDNF-AS ; BDNF
0.827 0.080 11 27693337 intron variant T/C snv 0.34 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1424266770
CASP3
0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 10
rs281865071
CHRNB2
0.882 0.080 1 154571759 missense variant C/G;T snv 5
rs80356702
CLCN1
0.882 0.120 7 143330868 missense variant G/A snv 4.0E-06 1.4E-05 9
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1556424691
CYTB ; ND6 ; TRNT
0.851 0.200 MT 15923 non coding transcript exon variant A/G snv 13
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs28937900
FKRP
0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 37
rs2732260
FUT10
0.882 0.200 8 33431749 intron variant G/A snv 8.4E-02 5
rs763868966
GFAP
1.000 0.080 17 44911429 stop gained C/A;G;T snv 1.2E-05; 4.0E-05 4
rs104894396
GJB2
0.672 0.400 13 20189511 stop gained C/T snv 5.8E-04 1.1E-04 28
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs370717845
HGSNAT
0.763 0.320 8 43161462 missense variant G/A snv 33
rs1977412
LOC105373166
0.882 0.160 1 230716523 intron variant T/A;C snv 5
rs1411832
LOC105378469
1.000 0.040 10 106126497 intergenic variant C/T snv 0.10 2