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
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs4818
COMT ; MIR4761
0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 25
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs52820871
MC4R
0.827 0.160 18 60371599 missense variant T/G snv 6.9E-03 7.6E-03 6
rs495225
GHSR
0.882 0.040 3 172448243 synonymous variant G/A;C;T snv 0.66 4
rs200889048 0.882 0.120 3 74928276 intergenic variant C/- del 3
rs554073050
CCK
0.925 0.040 3 42263460 synonymous variant G/A snv 1.2E-05 7.0E-06 3
rs12490016
LINC00880 ; LINC00881
0.882 0.120 3 157121142 intron variant G/C snv 4.6E-02 3
rs1042571
POMC
0.882 0.120 2 25161018 3 prime UTR variant G/A snv 0.16 3
rs1630623
TMC1
0.882 0.120 9 72725323 intron variant A/G snv 0.29 3
rs13338499
LOC101927837
0.925 0.040 16 67486220 intron variant A/G;T snv 2
rs77600076
CHODL
1.000 0.040 21 18159125 intron variant A/C snv 2.5E-02 1
rs287103
KCTD15
1.000 0.040 19 33801816 intron variant A/G snv 0.67 1
rs1445130
LOC105373456
1.000 0.040 2 18653385 regulatory region variant A/G snv 0.12 1
rs142014203
NKAIN3
1.000 0.040 8 62346358 intron variant T/G snv 2.1E-02 1