Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2619522
DTNBP1
0.827 0.080 6 15653418 intron variant A/C snv 0.26 6
rs28386840 0.827 0.080 16 55652906 upstream gene variant T/A;C snv 6
rs3789327
ARNTL
0.925 0.080 11 13363769 intron variant A/G snv 0.53 6
rs1106634
ATP6V1B2
0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs11111
GDNF-AS1 ; GDNF
0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 5
rs1187323
NTRK2
0.882 0.080 9 84668501 upstream gene variant C/A;G;T snv 5
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs12630592
GSK3B
0.851 0.080 3 120049399 intron variant G/A;T snv 5
rs12936511
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
0.925 0.080 17 45807036 synonymous variant C/T snv 3.1E-02 3.0E-02 5
rs13440581
GPR50
0.882 0.080 X 151181399 missense variant A/G snv 0.45 0.45 5
rs1415259
NOS1AP ; LOC105371475
0.925 0.080 1 162115519 intron variant C/T snv 0.54 5
rs174697
ARVCF ; COMT
0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs1799913
TPH1
0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs2070587
DAO
0.882 0.080 12 108883967 intron variant T/G snv 0.32 5
rs2072115
RAPGEF3
0.882 0.080 12 47751585 intron variant A/C;G snv 5
rs228697
PER3
0.882 0.080 1 7827519 missense variant C/G snv 8.7E-02 7.3E-02 5
rs3096140
GDNF ; GDNF-AS1
0.882 0.080 5 37832731 intron variant G/A snv 0.69 5
rs496250
FXR1
0.851 0.080 3 180909515 intron variant G/A snv 0.24 5
rs61888800
BDNF
0.851 0.080 11 27700731 5 prime UTR variant G/T snv 0.19 5
rs6903874 0.851 0.080 6 132575771 downstream gene variant T/C snv 0.23 5
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 5
rs794727961
CACNA1C
0.851 0.080 12 2512979 missense variant G/A snv 5
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47 5
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs10848635
CACNA1C
0.882 0.080 12 2207029 intron variant T/A;C snv 0.34 4