Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61888800
BDNF
0.851 0.080 11 27700731 5 prime UTR variant G/T snv 0.19 5
rs6857715
NPY2R ; LOC107986321
0.827 0.160 4 155208030 non coding transcript exon variant C/A;T snv 5
rs794727961
CACNA1C
0.851 0.080 12 2512979 missense variant G/A snv 5
rs796590326
P2RX7 ; LOC105370032
0.851 0.200 12 121162449 missense variant GT/AC mnv 5
rs945032
BDKRB2
0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 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
rs10447760 0.851 0.040 7 114083210 upstream gene variant C/T snv 0.17 4
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs10968749
LINGO2
0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 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
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 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
rs17790731
RFESD
0.851 0.040 5 95647825 5 prime UTR variant C/T snv 4.9E-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