Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3788533
PLA2G6
0.925 0.040 22 38127239 non coding transcript exon variant C/G snv 0.47 3
rs17075286 3 43189231 intergenic variant C/G snv 5.9E-02 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs989638
GRIA3
0.925 0.040 X 123239256 intron variant C/G;T snv 3
rs12282742
SAA2-SAA4 ; SAA2
11 18244252 intron variant C/G;T snv 2
rs7065696
PHF8
X 53947621 intron variant C/G;T snv 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 10
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 10
rs934945
PER2
0.827 0.200 2 238246412 missense variant C/T snv 0.21 0.15 10
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs1249144069
PITRM1-AS1 ; PITRM1
0.925 0.200 10 3165320 missense variant C/T snv 1.4E-05 5
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs2514218 0.925 0.040 11 113522272 regulatory region variant C/T snv 0.26 4
rs3916965 0.882 0.040 13 105451011 intergenic variant C/T snv 0.31 4
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs10494561
NMNAT2
1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 3
rs12105421
TMEM182
1.000 0.040 2 102959630 intron variant C/T snv 7.8E-02 2
rs12155594
NRG1
1.000 0.040 8 31749079 intron variant C/T snv 7.8E-02 2