Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs536599 1.000 0.080 4 46196917 intergenic variant G/T snv 0.47 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 7
rs141973904
ADH1B ; ADH1C
1.000 0.080 4 99341085 intron variant C/T snv 1.6E-02 1
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs916264
APOL2
1.000 0.080 22 36237790 intron variant A/C;T snv 1
rs7958822
ARNTL2
0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs4964057
ARNTL2
0.882 0.080 12 27363909 intron variant T/G snv 0.29 3
rs2306073
ARNTL2 ; ARNTL2-AS1
0.882 0.080 12 27402904 intron variant C/T snv 0.37 4
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs2412646
CLOCK ; TMEM165
0.882 0.120 4 55452605 3 prime UTR variant T/C snv 0.58 3
rs11240
CLOCK ; TMEM165
0.925 0.080 4 55453183 3 prime UTR variant C/A;G snv 2
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs3811939
CRHBP
1.000 0.080 5 76954762 intron variant G/A snv 0.27 2
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs4532
DRD1
0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 5
rs2119183
GABRA2
1.000 0.080 4 46270789 intron variant G/A snv 7.6E-02 2
rs3756007
GABRA2
1.000 0.080 4 46389047 5 prime UTR variant T/C snv 5.4E-02 2
rs11941860
GABRG1
1.000 0.080 4 46080161 intron variant C/T snv 0.12 2
rs17153694
GATA4
0.851 0.160 8 11730972 intron variant C/T snv 0.12 4
rs10112596
GATA4
0.925 0.120 8 11722293 intron variant A/G snv 0.83 3
rs11250159
GATA4
1.000 0.080 8 11729725 intron variant G/A;T snv 1