Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1519480
BDNF-AS
0.925 0.040 11 27654165 intron variant C/T snv 0.54 4
rs13316193
CAV3 ; OXTR
0.882 0.040 3 8761057 intron variant T/C snv 0.45 4
rs3758987
HTR3B
0.925 0.080 11 113904553 upstream gene variant T/C snv 0.32 4
rs9653711
LOC107985505 ; OLIG2
0.851 0.120 21 33029641 intron variant G/A;C snv 4
rs2857766
MOG
0.882 0.120 6 29666226 missense variant G/C snv 0.22 0.19 4
rs1059004
OLIG2
0.925 0.040 21 33028155 3 prime UTR variant C/A snv 0.41 4
rs2071592
ATP6V1G2-DDX39B ; ATP6V1G2 ; NFKBIL1
0.882 0.200 6 31547563 intron variant T/A;C snv 3
rs2268493
CAV3 ; OXTR
0.882 0.040 3 8759154 intron variant T/C snv 0.25 3
rs1805477
GRIN2B
0.882 0.080 12 13561795 3 prime UTR variant T/A;C;G snv 3
rs6517137
LOC107985505 ; OLIG2
0.882 0.120 21 33028471 3 prime UTR variant T/C snv 0.11 3
rs16965628
SLC6A4
0.882 0.040 17 30228407 intron variant G/C snv 0.14 3
rs28914832
SLC6A4
0.925 0.120 17 30211356 missense variant T/C;G snv 7.4E-04 3
rs2097603
TXNRD2 ; COMT
0.882 0.040 22 19940569 intron variant G/A;T snv 3
rs10070190 0.925 0.040 5 26866262 intergenic variant G/A snv 0.60 2
rs11783752 0.925 0.040 8 20192013 intergenic variant G/A;C snv 2
rs12504244 0.925 0.040 4 54619021 intergenic variant C/A;G;T snv 2
rs2834070 0.925 0.040 21 33015144 intron variant G/T snv 0.24 2
rs4785741 1.000 0.040 16 89939045 downstream gene variant T/C snv 0.47 2
rs75063949
CARMIL1
0.925 0.040 6 25590813 intron variant C/G snv 0.14 2
rs2268490
CAV3 ; OXTR
1.000 0.040 3 8755399 intron variant C/T snv 0.18 2
rs4686301
CAV3 ; OXTR
1.000 0.040 3 8756900 intron variant C/T snv 0.27 2
rs2289664
CDH2
0.925 0.120 18 27952340 missense variant T/C snv 2.5E-02 2.0E-02 2
rs2075507
COMT ; TXNRD2
0.925 0.040 22 19940569 intron variant G/A;T snv 2
rs11583978
DLGAP3
0.925 0.040 1 34864921 downstream gene variant A/C;G snv 2
rs4825476
GRIA3
0.925 0.040 X 123307628 intron variant G/A;C snv 2