Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 9
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs2268498
CAV3 ; OXTR
0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs2295633
FAAH
0.827 0.120 1 46408711 intron variant A/G;T snv 7
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 6
rs17689918
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.851 0.080 17 45832722 intron variant G/A snv 0.15 6
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs9804190
ANK3
0.882 0.040 10 60080073 intron variant C/T snv 0.30 5
rs386231
NOS1AP
0.882 0.080 1 162356033 intron variant C/T snv 0.68 4
rs9563121
KL
0.925 0.080 13 33050369 intron variant C/T snv 0.26 4
rs12944712
CRHR1 ; LINC02210-CRHR1
0.925 0.040 17 45793781 intron variant G/A snv 0.35 3