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
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs1805054
HTR6
0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs5930
MIR6886 ; LDLR
0.827 0.200 19 11113589 synonymous variant A/G snv 0.63 0.66 8
rs63750577
PSEN1
0.827 0.120 14 73186881 missense variant C/T snv 8
rs9875793 0.925 0.080 3 170968784 intron variant A/G snv 0.14 3
rs6494223
CHRNA7
0.882 0.120 15 32104256 intron variant C/T snv 0.43 3
rs10883866
NRG3
0.882 0.160 10 81883883 intron variant C/A;G;T snv 3
rs2153674
DAOA-AS1 ; DAOA
1.000 0.040 13 105478789 intron variant C/T snv 0.57 1
rs5905587
NDP
1.000 0.040 X 43974750 upstream gene variant T/C snv 1