Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 5
rs174697
ARVCF ; COMT
0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs231779
CTLA4
0.827 0.160 2 203869764 intron variant C/T snv 0.41 5
rs40184
SLC6A3
0.851 0.120 5 1394962 intron variant C/T snv 0.45 5
rs4512342
NRG1
0.827 0.120 8 32750356 intron variant T/G snv 0.12 5
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47 5
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs12649507
CLOCK
0.851 0.080 4 55514317 intron variant G/A;T snv 4
rs1401635
BDNF ; BDNF-AS
0.925 0.040 11 27672444 intron variant C/G snv 0.73 4
rs144733372
PLEKHM1
0.882 0.120 17 45486856 intron variant T/G snv 4
rs1488864
LOC101927825 ; CAVIN3
0.851 0.080 11 6321099 intron variant T/G snv 0.80 4
rs16875288
ADAMTS16 ; LOC101929200
0.851 0.040 5 5297087 intron variant A/T snv 0.22 4
rs16935279
LINC01592
0.851 0.040 8 68961217 intron variant T/C snv 1.9E-02 4
rs17158930
DOCK4
0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs17211233
RASGRF2
0.882 0.040 5 81072944 intron variant T/A;C snv 4
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs2199503
GSK3B
0.851 0.080 3 120059642 intron variant T/C snv 0.79 4
rs2273816
KPNA3
0.851 0.080 13 49719920 intron variant G/A;C snv 4
rs4238989
AANAT
0.851 0.120 17 76467306 intron variant C/G snv 0.45 4
rs4630333
TIMELESS
0.882 0.040 12 56443632 intron variant C/T snv 0.33 4
rs55945116
SEC11A
0.882 0.040 15 84676882 intron variant G/C snv 0.26 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs672607
BCL9
0.851 0.040 1 147581540 intron variant G/A snv 0.12 4
rs6740584
CREB1
0.882 0.040 2 207564627 intron variant T/C snv 0.37 4