Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs34177316
LOC107986273 ; APBB2
0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 3
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 7
rs9370822
DTNBP1 ; LOC105374947
0.882 0.120 6 15544505 intron variant A/C snv 0.36 7
rs11039409
NUP160
1.000 0.040 11 47814169 intron variant A/C snv 0.22 2
rs56403421 1.000 0.040 18 55098052 regulatory region variant A/C snv 0.26 2
rs600011
BBX
1.000 0.040 3 107576545 intron variant A/C snv 0.25 2
rs72788286
ATAD2B
1.000 0.040 2 23875451 intron variant A/C snv 0.12 2
rs77607745 1.000 0.040 13 69001052 intergenic variant A/C snv 0.15 2
rs878567
HTR1A
0.882 0.040 5 63960164 intron variant A/C;G snv 4
rs1875560
DCC
1.000 0.040 18 53434318 intron variant A/C;G snv 2
rs4713916
FKBP5
0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs9930139
RBFOX1
1.000 0.040 16 7239569 intron variant A/C;T snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs2271933
HCRTR1
0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50 9
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 6
rs1164376164
ABCB1
0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 6