Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1334496 1.000 0.040 X 137178554 intergenic variant C/A;T snv 1
rs4829605 1.000 0.040 X 137182822 intergenic variant C/A;G snv 1
rs11767557
EPHA1-AS1
0.882 0.080 7 143412046 intron variant T/C snv 0.18 4
rs111943087
CSF1R
0.925 0.080 5 150059725 missense variant G/A snv 1.4E-05 2
rs3756577
CAMK2A
0.925 0.080 5 150249081 intron variant C/T snv 0.14 2
rs3822606
CAMK2A
0.925 0.080 5 150261592 intron variant G/A snv 0.27 2
rs375752214
NOS3
0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs9340803
ESR1
0.925 0.080 6 151842832 intron variant A/G snv 1.0E-03 3.8E-04 2
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs640476 1.000 0.040 5 161277998 intergenic variant T/G snv 0.42 1
rs6850306
LCORL
0.925 0.080 4 18004466 intron variant G/A snv 0.12 2
rs12053868
IL1RAP
0.925 0.080 3 190582215 intron variant A/G snv 8.0E-02 2
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs63750048
PSEN2
0.925 0.080 1 226883817 missense variant C/T snv 4.0E-06 2
rs391300
SRR
0.882 0.160 17 2312964 intron variant T/C snv 0.58 4
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs9331888
CLU ; MIR6843
0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1451603364
BDNF-AS ; BDNF
0.925 0.120 11 27658411 missense variant C/T snv 4.0E-06 2
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs2534672
MICB
1.000 0.040 6 31497781 intron variant G/C snv 0.32 1
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82