Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs7958822
ARNTL2
0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs13212041
LOC105377864 ; HTR1B
0.851 0.200 6 77461407 downstream gene variant C/T snv 0.70 6
rs2306073
ARNTL2 ; ARNTL2-AS1
0.882 0.080 12 27402904 intron variant C/T snv 0.37 4
rs17110747
TPH2
0.882 0.120 12 72032174 3 prime UTR variant G/A snv 0.12 4
rs4964057
ARNTL2
0.882 0.080 12 27363909 intron variant T/G snv 0.29 3
rs1034936
CACNA1C
0.882 0.080 12 2551994 intron variant C/T snv 0.61 3
rs6350
SLC6A3
0.882 0.080 5 1443084 missense variant G/A;C snv 5.6E-02; 6.8E-05 3
rs2567608
SSTR4
0.925 0.080 20 23036445 missense variant T/A;C snv 2.8E-05; 0.49 2
rs348449
ALDH1A1
1.000 0.080 9 72940066 intron variant G/A snv 0.94 1
rs12655166
NR3C1
1.000 0.080 5 143429707 intron variant T/C snv 0.19 1